CS208133B2 - Selective herbicide means and method of making the active component of the same - Google Patents
Selective herbicide means and method of making the active component of the same Download PDFInfo
- Publication number
- CS208133B2 CS208133B2 CS795886A CS588679A CS208133B2 CS 208133 B2 CS208133 B2 CS 208133B2 CS 795886 A CS795886 A CS 795886A CS 588679 A CS588679 A CS 588679A CS 208133 B2 CS208133 B2 CS 208133B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- alpha
- acid
- phenyl
- ester
- cyano
- Prior art date
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- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 8
- 239000004009 herbicide Substances 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title description 2
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- 150000001875 compounds Chemical class 0.000 claims abstract description 36
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- CRANTQWPQYPOLF-UHFFFAOYSA-N [3-(ethanethioylamino)phenyl] N-(1-cyano-2-phenylpropyl)-N-methylcarbamate Chemical compound CC(=S)NC=1C=C(C=CC1)OC(N(C)C(C(C)C1=CC=CC=C1)C#N)=O CRANTQWPQYPOLF-UHFFFAOYSA-N 0.000 description 1
- JVAKWCYJXPJMSZ-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-(1-cyano-2-phenylethyl)-N-methylcarbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C)C(CC1=CC=CC=C1)C#N)=O JVAKWCYJXPJMSZ-UHFFFAOYSA-N 0.000 description 1
- RKOAGOKMTZXHPL-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] N-[cyano(phenyl)methyl]-N-methylcarbamate Chemical compound COC(=O)NC=1C=C(C=CC1)OC(N(C)C(C1=CC=CC=C1)C#N)=O RKOAGOKMTZXHPL-UHFFFAOYSA-N 0.000 description 1
- QMYZVJWFQUSLKT-UHFFFAOYSA-N [3-(prop-2-ynoxycarbonylamino)phenyl] N-(1-cyano-2-phenylpropyl)-N-methylcarbamate Chemical compound C(C#C)OC(=O)NC=1C=C(C=CC=1)OC(N(C)C(C(C)C1=CC=CC=C1)C#N)=O QMYZVJWFQUSLKT-UHFFFAOYSA-N 0.000 description 1
- YJPWLDJMVCBNTK-UHFFFAOYSA-N [3-(propan-2-yloxycarbonylamino)phenyl] N-(1-cyano-2-phenylpropyl)-N-methylcarbamate Chemical compound CC(C)OC(=O)NC=1C=C(C=CC1)OC(N(C)C(C(C)C1=CC=CC=C1)C#N)=O YJPWLDJMVCBNTK-UHFFFAOYSA-N 0.000 description 1
- UGYCPIDQOKQBLO-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(1-cyano-2-phenylethyl)-N-methylcarbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C)C(CC1=CC=CC=C1)C#N)=O UGYCPIDQOKQBLO-UHFFFAOYSA-N 0.000 description 1
- UAOBJWZXQIDRHX-UHFFFAOYSA-N [3-(propanethioylamino)phenyl] N-(1-cyano-2-phenylpropyl)-N-methylcarbamate Chemical compound C(C)C(=S)NC=1C=C(C=CC1)OC(N(C)C(C(C)C1=CC=CC=C1)C#N)=O UAOBJWZXQIDRHX-UHFFFAOYSA-N 0.000 description 1
- URPYCTBOIGRCLD-UHFFFAOYSA-N [cyano(phenyl)methyl]-ethylcarbamic acid Chemical compound CCN(C(C#N)C1=CC=CC=C1)C(O)=O URPYCTBOIGRCLD-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- AFVLVVWMAFSXCK-VMPITWQZSA-N alpha-cyano-4-hydroxycinnamic acid Chemical group OC(=O)C(\C#N)=C\C1=CC=C(O)C=C1 AFVLVVWMAFSXCK-VMPITWQZSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- YALDBVFQBATWNS-UHFFFAOYSA-N benzyl(1-cyanoethyl)carbamic acid Chemical compound N#CC(C)N(C(O)=O)CC1=CC=CC=C1 YALDBVFQBATWNS-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 125000006630 butoxycarbonylamino group Chemical group 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 229940112021 centrally acting muscle relaxants carbamic acid ester Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000021438 curry Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002168 ethanoic acid esters Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000006626 methoxycarbonylamino group Chemical group 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229950004864 olamine Drugs 0.000 description 1
- 150000007530 organic bases Chemical group 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782843691 DE2843691A1 (de) | 1978-10-04 | 1978-10-04 | Diurethane, verfahren zur herstellung dieser verbindungen sowie diese enthaltende selektive herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS208133B2 true CS208133B2 (en) | 1981-08-31 |
Family
ID=6051610
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS795886A CS208133B2 (en) | 1978-10-04 | 1979-08-29 | Selective herbicide means and method of making the active component of the same |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US4257803A (de) |
| JP (1) | JPS5820952B2 (de) |
| AR (1) | AR222349A1 (de) |
| AT (1) | AT365894B (de) |
| AU (1) | AU525979B2 (de) |
| BE (1) | BE879202A (de) |
| BR (1) | BR7906367A (de) |
| CA (1) | CA1122998A (de) |
| CH (1) | CH641769A5 (de) |
| CS (1) | CS208133B2 (de) |
| DD (1) | DD157755A5 (de) |
| DE (1) | DE2843691A1 (de) |
| EG (1) | EG13807A (de) |
| ES (1) | ES484476A1 (de) |
| FI (1) | FI792896A7 (de) |
| FR (1) | FR2438032A1 (de) |
| GB (1) | GB2032916B (de) |
| GR (1) | GR73017B (de) |
| HU (1) | HU185371B (de) |
| IL (1) | IL58372A (de) |
| IN (1) | IN153098B (de) |
| IT (1) | IT1163725B (de) |
| MA (1) | MA18593A1 (de) |
| MX (1) | MX5707E (de) |
| NL (1) | NL7905935A (de) |
| PH (1) | PH15068A (de) |
| PL (1) | PL117893B1 (de) |
| PT (1) | PT70247A (de) |
| RO (1) | RO78854A (de) |
| SE (1) | SE7908190L (de) |
| SU (1) | SU942586A3 (de) |
| TR (1) | TR20532A (de) |
| YU (1) | YU214179A (de) |
| ZA (1) | ZA795302B (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0051564A1 (de) * | 1980-10-31 | 1982-05-12 | Ciba-Geigy Ag | Neue Carbamate |
| JPS58176770A (ja) * | 1982-04-09 | 1983-10-17 | Fujitsu Ltd | 投票券発売機 |
| DE102009002248A1 (de) * | 2009-04-07 | 2010-10-14 | Max Bögl Bauunternehmung GmbH & Co. KG | Verfahren zum Errichten einer Off-Shore-Anlage und Off-Shore-Anlage |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3036112A (en) * | 1959-09-15 | 1962-05-22 | Union Carbide Corp | Bis(cyanoalkyl) phenylenedicarbamates |
| DE1567151C3 (de) | 1965-04-09 | 1974-02-21 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende herbizide Mittel |
| US3551477A (en) * | 1966-07-06 | 1970-12-29 | Basf Ag | Novel biscarbamates |
| DE2630418A1 (de) * | 1976-07-02 | 1978-01-05 | Schering Ag | Carbanilsaeureester, verfahren zur herstellung dieser verbindungen sowie diese enthaltende herbizide mittel |
-
1978
- 1978-10-04 DE DE19782843691 patent/DE2843691A1/de not_active Withdrawn
-
1979
- 1979-08-01 NL NL7905935A patent/NL7905935A/nl not_active Application Discontinuation
- 1979-08-24 IN IN603/DEL/79A patent/IN153098B/en unknown
- 1979-08-29 CS CS795886A patent/CS208133B2/cs unknown
- 1979-08-31 MX MX798358U patent/MX5707E/es unknown
- 1979-09-03 YU YU02141/79A patent/YU214179A/xx unknown
- 1979-09-17 GB GB7932155A patent/GB2032916B/en not_active Expired
- 1979-09-18 FI FI792896A patent/FI792896A7/fi not_active Application Discontinuation
- 1979-09-24 MA MA18793A patent/MA18593A1/fr unknown
- 1979-09-26 ES ES484476A patent/ES484476A1/es not_active Expired
- 1979-09-28 TR TR20532A patent/TR20532A/xx unknown
- 1979-09-28 PT PT70247A patent/PT70247A/pt unknown
- 1979-10-01 SU SU792824003A patent/SU942586A3/ru active
- 1979-10-01 DD DDAPA01N/215932A patent/DD157755A5/de unknown
- 1979-10-02 CA CA336,847A patent/CA1122998A/en not_active Expired
- 1979-10-02 PL PL1979218688A patent/PL117893B1/pl unknown
- 1979-10-02 GR GR60164A patent/GR73017B/el unknown
- 1979-10-03 SE SE7908190A patent/SE7908190L/ not_active Application Discontinuation
- 1979-10-03 BR BR7906367A patent/BR7906367A/pt unknown
- 1979-10-03 PH PH23105A patent/PH15068A/en unknown
- 1979-10-03 AT AT0646079A patent/AT365894B/de not_active IP Right Cessation
- 1979-10-03 IT IT26209/79A patent/IT1163725B/it active
- 1979-10-03 EG EG582/79A patent/EG13807A/xx active
- 1979-10-03 AU AU51425/79A patent/AU525979B2/en not_active Ceased
- 1979-10-03 US US06/081,320 patent/US4257803A/en not_active Expired - Lifetime
- 1979-10-03 HU HU79SCHE693A patent/HU185371B/hu unknown
- 1979-10-03 IL IL58372A patent/IL58372A/xx unknown
- 1979-10-04 AR AR278361A patent/AR222349A1/es active
- 1979-10-04 CH CH895679A patent/CH641769A5/de not_active IP Right Cessation
- 1979-10-04 BE BE0/197475A patent/BE879202A/fr not_active IP Right Cessation
- 1979-10-04 FR FR7924682A patent/FR2438032A1/fr active Pending
- 1979-10-04 ZA ZA00795302A patent/ZA795302B/xx unknown
- 1979-10-04 RO RO7998851A patent/RO78854A/ro unknown
- 1979-10-04 JP JP54127423A patent/JPS5820952B2/ja not_active Expired
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