DE970322C - Mittel zur Beeinflussung des Pflanzenwachstums - Google Patents
Mittel zur Beeinflussung des PflanzenwachstumsInfo
- Publication number
- DE970322C DE970322C DEG15250A DEG0015250A DE970322C DE 970322 C DE970322 C DE 970322C DE G15250 A DEG15250 A DE G15250A DE G0015250 A DEG0015250 A DE G0015250A DE 970322 C DE970322 C DE 970322C
- Authority
- DE
- Germany
- Prior art keywords
- carbamate
- phenyl
- methyl
- dimethyl
- tert
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 230000008635 plant growth Effects 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 238000009826 distribution Methods 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims 1
- 229910052736 halogen Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- -1 alkyl radical Chemical class 0.000 description 31
- 239000004480 active ingredient Substances 0.000 description 17
- 241000196324 Embryophyta Species 0.000 description 14
- 238000005520 cutting process Methods 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- APRJFNLVTJWEPP-UHFFFAOYSA-M n,n-diethylcarbamate Chemical compound CCN(CC)C([O-])=O APRJFNLVTJWEPP-UHFFFAOYSA-M 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
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- 239000002904 solvent Substances 0.000 description 4
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 3
- 230000002786 root growth Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000004936 stimulating effect Effects 0.000 description 3
- OOSBSVDOHPTTCT-UHFFFAOYSA-N (2,4-dichlorophenoxy)-methoxy-methyl-sulfanylidene-$l^{5}-phosphane Chemical group COP(C)(=S)OC1=CC=C(Cl)C=C1Cl OOSBSVDOHPTTCT-UHFFFAOYSA-N 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
- LKVFCSWBKOVHAH-UHFFFAOYSA-N 4-Ethoxyphenol Chemical compound CCOC1=CC=C(O)C=C1 LKVFCSWBKOVHAH-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 241001101998 Galium Species 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- QCOGKXLOEWLIDC-UHFFFAOYSA-N N-methylbutylamine Chemical compound CCCCNC QCOGKXLOEWLIDC-UHFFFAOYSA-N 0.000 description 2
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
- 239000003621 irrigation water Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- DWLVWMUCHSLGSU-UHFFFAOYSA-M n,n-dimethylcarbamate Chemical compound CN(C)C([O-])=O DWLVWMUCHSLGSU-UHFFFAOYSA-M 0.000 description 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- NRZWYNLTFLDQQX-UHFFFAOYSA-N p-tert-Amylphenol Chemical compound CCC(C)(C)C1=CC=C(O)C=C1 NRZWYNLTFLDQQX-UHFFFAOYSA-N 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- QICKOOCQSYZYQB-UHFFFAOYSA-N (4-hydroxyphenyl)thiourea Chemical compound NC(=S)NC1=CC=C(O)C=C1 QICKOOCQSYZYQB-UHFFFAOYSA-N 0.000 description 1
- MHVJUTLRTHDAOG-UHFFFAOYSA-N (4-hydroxyphenyl)urea Chemical compound NC(=O)NC1=CC=C(O)C=C1 MHVJUTLRTHDAOG-UHFFFAOYSA-N 0.000 description 1
- XNHCGFLXFHEXBN-UHFFFAOYSA-N (4-methylphenyl) morpholine-4-carboxylate Chemical compound C1=CC(C)=CC=C1OC(=O)N1CCOCC1 XNHCGFLXFHEXBN-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- HFZWRUODUSTPEG-UHFFFAOYSA-N 2,4-dichlorophenol Chemical compound OC1=CC=C(Cl)C=C1Cl HFZWRUODUSTPEG-UHFFFAOYSA-N 0.000 description 1
- RANCECPPZPIPNO-UHFFFAOYSA-N 2,5-dichlorophenol Chemical compound OC1=CC(Cl)=CC=C1Cl RANCECPPZPIPNO-UHFFFAOYSA-N 0.000 description 1
- KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical group COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- MOEFFSWKSMRFRQ-UHFFFAOYSA-N 2-ethoxyphenol Chemical compound CCOC1=CC=CC=C1O MOEFFSWKSMRFRQ-UHFFFAOYSA-N 0.000 description 1
- CRBJBYGJVIBWIY-UHFFFAOYSA-N 2-isopropylphenol Chemical class CC(C)C1=CC=CC=C1O CRBJBYGJVIBWIY-UHFFFAOYSA-N 0.000 description 1
- WDNBURPWRNALGP-UHFFFAOYSA-N 3,4-Dichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1 WDNBURPWRNALGP-UHFFFAOYSA-N 0.000 description 1
- ZDWSNKPLZUXBPE-UHFFFAOYSA-N 3,5-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1 ZDWSNKPLZUXBPE-UHFFFAOYSA-N 0.000 description 1
- MESJRHHDBDCQTH-UHFFFAOYSA-N 3-(dimethylamino)phenol Chemical compound CN(C)C1=CC=CC(O)=C1 MESJRHHDBDCQTH-UHFFFAOYSA-N 0.000 description 1
- VGIJZDWQVCXVNL-UHFFFAOYSA-N 3-butoxyphenol Chemical compound CCCCOC1=CC=CC(O)=C1 VGIJZDWQVCXVNL-UHFFFAOYSA-N 0.000 description 1
- XBRTZCAOTXIODV-UHFFFAOYSA-N 4-(3-methylbutylsulfanyl)phenol Chemical compound CC(C)CCSC1=CC=C(O)C=C1 XBRTZCAOTXIODV-UHFFFAOYSA-N 0.000 description 1
- KDWPYZPZUPWJGB-UHFFFAOYSA-N 4-(4-chlorophenyl)morpholine Chemical compound C1=CC(Cl)=CC=C1N1CCOCC1 KDWPYZPZUPWJGB-UHFFFAOYSA-N 0.000 description 1
- QASBCTGZKABPKX-UHFFFAOYSA-N 4-(methylsulfanyl)phenol Chemical compound CSC1=CC=C(O)C=C1 QASBCTGZKABPKX-UHFFFAOYSA-N 0.000 description 1
- KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 1
- GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- CYYZDBDROVLTJU-UHFFFAOYSA-N 4-n-Butylphenol Chemical compound CCCCC1=CC=C(O)C=C1 CYYZDBDROVLTJU-UHFFFAOYSA-N 0.000 description 1
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
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- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
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- DNUTZBZXLPWRJG-UHFFFAOYSA-M piperidine-1-carboxylate Chemical compound [O-]C(=O)N1CCCCC1 DNUTZBZXLPWRJG-UHFFFAOYSA-M 0.000 description 1
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- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/205—Radicals derived from carbonic acid
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01H—SPINNING OR TWISTING
- D01H5/00—Drafting machines or arrangements ; Threading of roving into drafting machine
- D01H5/18—Drafting machines or arrangements without fallers or like pinned bars
- D01H5/70—Constructional features of drafting elements
- D01H5/74—Rollers or roller bearings
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01H—SPINNING OR TWISTING
- D01H2700/00—Spinning or twisting machines; Drafting devices
- D01H2700/245—Conception or fabrication of drafting cylinders
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Plant Pathology (AREA)
- Textile Engineering (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH2776196X | 1953-09-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE970322C true DE970322C (de) | 1958-09-04 |
Family
ID=4571693
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEG15250A Expired DE970322C (de) | 1953-09-02 | 1954-09-02 | Mittel zur Beeinflussung des Pflanzenwachstums |
Country Status (5)
| Country | Link |
|---|---|
| US (3) | US2812247A (en, 2012) |
| BE (1) | BE531554A (en, 2012) |
| DE (1) | DE970322C (en, 2012) |
| FR (1) | FR1112804A (en, 2012) |
| NL (1) | NL190462A (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1101046B (de) * | 1959-05-08 | 1961-03-02 | Hoechst Ag | N-(Perchlorylphenyl)-alkyl-carbamate als Mittel zur Regulierung des Pflanzenwachstums |
Families Citing this family (82)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3271442A (en) * | 1955-08-29 | 1966-09-06 | Union Carbide Corp | 5-acenaphthenyl esters of carbamic acid and nu-substituted alkyl carbamic acids |
| US2893856A (en) * | 1956-03-23 | 1959-07-07 | Monsanto Chemicals | Defoliating compositions |
| US2933383A (en) * | 1956-11-23 | 1960-04-19 | Union Carbide Corp | Method of combating weeds using nu-substituted carbamates of 2, 4, 5-trichloro, 6-nitro phenol |
| US2977209A (en) * | 1957-02-13 | 1961-03-28 | Stauffer Chemical Co | Method of combatting weeds |
| US2992091A (en) * | 1957-05-06 | 1961-07-11 | Monsanto Chemicals | Method of controlling undesirable vegetation |
| GB828871A (en) * | 1957-07-12 | 1960-02-24 | Shell Res Ltd | Herbicidal compositions |
| NL236579A (en, 2012) * | 1958-02-01 | |||
| BE587481A (en, 2012) * | 1958-08-07 | |||
| US3062865A (en) * | 1959-06-08 | 1962-11-06 | California Research Corp | M-sec. butylphenyl n-methylcarbamate |
| US3062866A (en) * | 1959-06-08 | 1962-11-06 | California Research Corp | M-(1-methylhexyl)phenyl n-methylcarbamate |
| US3062867A (en) * | 1959-06-08 | 1962-11-06 | California Research Corp | M-(1-ethylpropyl) phenyl n-methyl-carbamate |
| US3062707A (en) * | 1959-06-29 | 1962-11-06 | California Research Corp | 3-t-amyl-6-chlorophenyl n-methylcarbamate and method of inhibiting the cholinesterase function in agricultural parasites therewith |
| US3062864A (en) * | 1959-06-08 | 1962-11-06 | California Research Corp | M-(1-methylbutyl)phenyl n-methylcarbamate |
| US3062868A (en) * | 1959-06-29 | 1962-11-06 | California Research Corp | 3-t-amyl-6-bromophenyl n-methylcarbamate |
| US3066163A (en) * | 1959-06-29 | 1962-11-27 | California Research Corp | M-(1-methylpentyl) phenyl n-methylcarbamate |
| NL254339A (en, 2012) * | 1959-07-31 | |||
| US3110726A (en) * | 1959-09-21 | 1963-11-12 | Joseph E Moore | Mu-(1-cyclopropylethyl) phenyl nu-methylcarbamate |
| US3053895A (en) * | 1959-11-04 | 1962-09-11 | Dow Chemical Co | Unsymmetrical dialkylaminophenols |
| BE597390A (en, 2012) * | 1959-11-24 | |||
| US3313684A (en) * | 1959-12-05 | 1967-04-11 | Bayer Ag | 3, 5-dimethyl-4-methylmercaptophenyl n-methyl carbamate and methods for combating insects |
| BE600153A (en, 2012) * | 1960-02-13 | |||
| NL266053A (en, 2012) * | 1960-06-17 | |||
| US3076741A (en) * | 1960-06-20 | 1963-02-05 | California Research Corp | 3-sec. butyl-6-chlorophenyl n-methylcarbamate and use thereof as a pesticide |
| BE606036A (en, 2012) * | 1960-07-12 | |||
| US3328154A (en) * | 1960-09-12 | 1967-06-27 | Monsanto Co | Destroying undesired vegetation with halobenzylcarbamates |
| US3131215A (en) * | 1960-10-06 | 1964-04-28 | Upjohn Co | 2-halo-and 2, 4-dihalo-alkylphenyl carbamates |
| US3081340A (en) * | 1960-12-30 | 1963-03-12 | Union Carbide Corp | Dihydronaphthyl n-methyl-carbamates |
| US3275507A (en) * | 1960-12-30 | 1966-09-27 | Union Carbide Corp | Aminonaphthyl and alkylaminonaphthyl n-methylcarbamates and insecticidal compositions thereof |
| US3099681A (en) * | 1960-12-30 | 1963-07-30 | Union Carbide Corp | 5-lower acylamino 1-naphthyl n-methylcarbamates |
| NL272564A (en, 2012) * | 1960-12-30 | |||
| US3197364A (en) * | 1960-12-30 | 1965-07-27 | Union Carbide Corp | Substituted 1-naphthyl n-methylcarbamate insecticide |
| US3236877A (en) * | 1960-12-30 | 1966-02-22 | Union Carbide Corp | 5-(amino, alkylamino and aralkylamino naphthyl) n-methylcarbamates |
| FR1310198A (en, 2012) * | 1961-01-25 | 1963-03-06 | ||
| US3211770A (en) * | 1961-04-03 | 1965-10-12 | Diamond Alkali Co | 5, 5, 5 trihalo-2-pentenyl carbamates |
| US3202573A (en) * | 1961-05-31 | 1965-08-24 | Hercules Powder Co Ltd | Propargoxyphenyl nu-methylcarbamates and their use as pesticides |
| US3109006A (en) * | 1961-07-03 | 1963-10-29 | Monsanto Chemicals | Benzyl heterocyclicamino-carbothiolates |
| US3142556A (en) * | 1961-09-18 | 1964-07-28 | Monsanto Co | Controlling vegetation with pyrrolidinylcarboxylates |
| US3341401A (en) * | 1961-12-11 | 1967-09-12 | Union Carbide Corp | Halo-meta-isopropylphenyl n-methylcarbamates and pesticidal compositions |
| US3358012A (en) * | 1962-02-16 | 1967-12-12 | Allied Chem | 3-isopropyl-4-methylmercaptophenyl nu-methylcarbamate |
| US3139333A (en) * | 1962-03-05 | 1964-06-30 | Fmc Corp | Method for regulating fruit set |
| NL291251A (en, 2012) * | 1962-04-09 | |||
| US3140167A (en) * | 1962-06-07 | 1964-07-07 | Hercules Powder Co Ltd | 2, 6-di-t-butyl-4-substituted phenyl nu-methyl carbamate and use thereof as selective herbicides |
| US3297680A (en) * | 1962-09-26 | 1967-01-10 | Monsanto Co | Haloalkenyl disubstituted thionocarbamates |
| US3377375A (en) * | 1963-02-07 | 1968-04-09 | Monsanto Co | N-aralkylsulfonyl carbamates |
| US3349115A (en) * | 1963-02-19 | 1967-10-24 | Hooker Chemical Corp | Sulfur-containing carbamate insecticides |
| US3349116A (en) * | 1963-02-20 | 1967-10-24 | Hooker Chemical Corp | Ortho hydrocarbyloxy alkenylenephenyl nu-lower alkylcarbamates |
| DE1567204B1 (de) * | 1963-04-02 | 1971-10-14 | Union Carbide Corp | Chlorbenzyl-N-methylcarbamate und diese enthaltende Herbizide |
| US3238036A (en) * | 1963-04-02 | 1966-03-01 | Union Carbide Corp | Method of inhibiting plant growth with cyclohexenyl carbamates |
| US3361556A (en) * | 1963-09-03 | 1968-01-02 | Du Pont | Method for preparing seed for establishing a perennial grass turf |
| US3345155A (en) * | 1963-09-03 | 1967-10-03 | Du Pont | Establishing perennial grass turf with cycloalkyl esters of a carbanilic acid |
| US3434822A (en) * | 1964-03-23 | 1969-03-25 | Fmc Corp | M-ureidophenyl carbamates as herbicides |
| DE1254617B (de) * | 1964-06-27 | 1967-11-23 | Bayer Ag | Verfahren zur Herstellung von N-Methyl-O-phenylcarbaminsaeureestern |
| DE1248635B (de) * | 1964-07-04 | 1967-08-31 | Farbenfabriken Bayer Aktiengesellschaft, Leverkusen | Verfahren zur Herstellung eines Alkenylmercaptophenyl - N - methyl-carbaminsäureesters |
| NL6408165A (en, 2012) * | 1964-07-17 | 1966-01-18 | ||
| US3388991A (en) * | 1964-08-12 | 1968-06-18 | Monsanto Co | Method of controlling undesired vegetation with polychlorophenyl nu-allyl-nu-cyclohexylcarbamates |
| US3253904A (en) * | 1965-03-15 | 1966-05-31 | Du Pont | Composition and method for desuckering tobacco |
| US3340294A (en) * | 1965-05-10 | 1967-09-05 | Velsicol Chemical Corp | N-substituted and unsubstituted alkyl and alkenyl-2-dimethylamino-benzhydrylcarbamates |
| US3442889A (en) * | 1965-06-14 | 1969-05-06 | Monsanto Co | Halobenzyl carbamates |
| CH457400A (de) * | 1965-06-25 | 1968-06-15 | Agripat Sa | Verfahren zur Herstellung neuer Carbaminsäureester und ihre Verwendung zur Bekämpfung von Schädlingen |
| US3857693A (en) * | 1965-10-14 | 1974-12-31 | Fmc Corp | Anilide carbamates as herbicides |
| US3425820A (en) * | 1966-03-21 | 1969-02-04 | Hodogaya Chemical Co Ltd | Herbicidal composition |
| US3341404A (en) * | 1966-03-31 | 1967-09-12 | Union Carbide Corp | Method of killing insects with 5, 6, 7, 8-tetrahydro-1-naphthyl-n-methyl carbamate |
| US3876684A (en) * | 1966-09-06 | 1975-04-08 | Fmc Corp | M-amidophenyl n-substituted carbamates |
| CH489999A (de) * | 1966-12-01 | 1970-05-15 | Ciba Geigy | Schädlingsbekämpfungsmittel |
| US3439021A (en) * | 1966-12-23 | 1969-04-15 | Stauffer Chemical Co | Halo-substituted phenoxyethyl carbamates and derivatives thereof |
| US3683007A (en) * | 1967-04-20 | 1972-08-08 | Du Pont | Alkyl-n-(4-alkyl-or cycloalkyl-methyl cyclohexyl) carbamates |
| US3919289A (en) * | 1967-05-08 | 1975-11-11 | Us Army | Carbamates |
| CH506494A (de) * | 1967-08-22 | 1971-04-30 | Ciba Geigy Ag | Verfahren zur Herstellung von substituierten Aminophenylcarbamaten |
| US3455673A (en) * | 1967-12-08 | 1969-07-15 | Smithkline Corp | Compositions and methods for regulating the growth of plants |
| US3529953A (en) * | 1968-02-01 | 1970-09-22 | Raymond W Luckenbaugh | Cyclooctyl - 2 - ene - 1 - ol esters of substituted carbanilic acids as selective herbicides |
| US3511875A (en) * | 1968-04-12 | 1970-05-12 | Du Pont | Herbicidal alkylcarbamoyloxy semicarbazides |
| US3532738A (en) * | 1968-06-03 | 1970-10-06 | Fmc Corp | Ureidophenyl carbamates |
| US3938986A (en) * | 1969-03-17 | 1976-02-17 | Ppg Industries, Inc. | Herbicide |
| US3726910A (en) * | 1970-04-01 | 1973-04-10 | Dow Chemical Co | (((alkylthio)alkyl)thio)phenyl carbamates |
| US3874939A (en) * | 1971-05-28 | 1975-04-01 | Ppg Industries Inc | Herbicidal compositions containing cycloalkyl carbamates as soil life extenders |
| US3871866A (en) * | 1971-06-01 | 1975-03-18 | Ppg Industries Inc | Herbicide and method for controlling weeds |
| US4772744A (en) * | 1972-03-14 | 1988-09-20 | Rohm And Haas Company | Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers |
| DE2545389A1 (de) * | 1974-10-15 | 1976-04-29 | Mitsubishi Chem Ind | Carbamat-derivate, verfahren zur deren herstellung und deren verwendung, insbesondere als insektizide |
| US4303793A (en) * | 1979-03-12 | 1981-12-01 | Ppg Industries, Inc. | Aqueous carbamate dispersions |
| US4390710A (en) * | 1981-10-19 | 1983-06-28 | Ppg Industries, Inc. | Catalyst system for manufacturing p-chlorophenyl-N-methyl carbamate |
| US5194661A (en) * | 1990-08-20 | 1993-03-16 | Ici Americas Inc. | Substituted benzyl carbamates and their use as herbicides |
| JP4515911B2 (ja) * | 2002-10-07 | 2010-08-04 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | アナンダミド加水分解の遮断による不安の調節 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2208485A (en) * | 1937-04-24 | 1940-07-16 | Hoffmann La Roche | Process for the manufacture of disubstituted carbamic acid esters of phenols containing a basic substituent |
| US2412510A (en) * | 1944-06-02 | 1946-12-10 | American Chem Paint Co | Methods and compositions for killing weeds |
| US2493710A (en) * | 1947-03-21 | 1950-01-03 | Hoffmann La Roche | Carbamic acid esters |
| US2677698A (en) * | 1950-08-01 | 1954-05-04 | Spencer Chem Co | Preparation of nu-monosubstituted carbamic acid esters |
-
0
- BE BE531554D patent/BE531554A/xx unknown
- NL NL190462D patent/NL190462A/xx unknown
-
1953
- 1953-12-14 US US398186A patent/US2812247A/en not_active Expired - Lifetime
-
1954
- 1954-08-23 US US451718A patent/US2776197A/en not_active Expired - Lifetime
- 1954-08-23 US US451719A patent/US2776196A/en not_active Expired - Lifetime
- 1954-09-02 DE DEG15250A patent/DE970322C/de not_active Expired
- 1954-09-02 FR FR1112804D patent/FR1112804A/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1101046B (de) * | 1959-05-08 | 1961-03-02 | Hoechst Ag | N-(Perchlorylphenyl)-alkyl-carbamate als Mittel zur Regulierung des Pflanzenwachstums |
Also Published As
| Publication number | Publication date |
|---|---|
| US2776196A (en) | 1957-01-01 |
| US2776197A (en) | 1957-01-01 |
| FR1112804A (fr) | 1956-03-19 |
| US2812247A (en) | 1957-11-05 |
| NL190462A (en, 2012) | |
| BE531554A (en, 2012) |
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