PL125385B1 - Herbicide - Google Patents
Herbicide Download PDFInfo
- Publication number
- PL125385B1 PL125385B1 PL1981230201A PL23020181A PL125385B1 PL 125385 B1 PL125385 B1 PL 125385B1 PL 1981230201 A PL1981230201 A PL 1981230201A PL 23020181 A PL23020181 A PL 23020181A PL 125385 B1 PL125385 B1 PL 125385B1
- Authority
- PL
- Poland
- Prior art keywords
- compound
- group
- compounds
- methyl
- chloroacetanilide
- Prior art date
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- 230000002363 herbicidal effect Effects 0.000 title claims description 74
- 239000004009 herbicide Substances 0.000 title claims description 69
- 150000001875 compounds Chemical class 0.000 claims description 253
- 239000003795 chemical substances by application Substances 0.000 claims description 41
- 239000013543 active substance Substances 0.000 claims description 28
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 25
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 22
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 19
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 7
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims description 6
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 6
- VFTAWPWOQOKZQU-UHFFFAOYSA-N 2-chloro-n-(2-methyl-6-propan-2-yloxyphenyl)-n-(2-methylpropoxymethyl)acetamide Chemical compound CC(C)COCN(C(=O)CCl)C1=C(C)C=CC=C1OC(C)C VFTAWPWOQOKZQU-UHFFFAOYSA-N 0.000 claims description 3
- VGENZFWQPCCFCZ-UHFFFAOYSA-N 2-chloro-n-[2-methyl-6-(2-methylpropoxy)phenyl]-n-(propan-2-yloxymethyl)acetamide Chemical compound CC(C)COC1=CC=CC(C)=C1N(COC(C)C)C(=O)CCl VGENZFWQPCCFCZ-UHFFFAOYSA-N 0.000 claims description 3
- KBDPMAIYQDDLRP-UHFFFAOYSA-N 2-chloro-n-[2-methyl-6-(2-methylpropoxy)phenyl]-n-(propoxymethyl)acetamide Chemical compound CCCOCN(C(=O)CCl)C1=C(C)C=CC=C1OCC(C)C KBDPMAIYQDDLRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- YXYSLCGLFIEUTK-UHFFFAOYSA-N 2-chloro-n-(2-methylpropoxymethyl)-n-(2-methyl-6-propoxyphenyl)acetamide Chemical compound CCCOC1=CC=CC(C)=C1N(COCC(C)C)C(=O)CCl YXYSLCGLFIEUTK-UHFFFAOYSA-N 0.000 claims description 2
- DRHUVSGQJXFFFC-UHFFFAOYSA-N n-(2-butoxy-6-ethylphenyl)-2-chloro-n-(propoxymethyl)acetamide Chemical compound CCCCOC1=CC=CC(CC)=C1N(COCCC)C(=O)CCl DRHUVSGQJXFFFC-UHFFFAOYSA-N 0.000 claims description 2
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- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 7
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- 125000003545 alkoxy group Chemical group 0.000 description 4
- 150000003931 anilides Chemical group 0.000 description 4
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 4
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
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- 239000005909 Kieselgur Substances 0.000 description 3
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- RQTDRJMAUKHGHV-UHFFFAOYSA-N P.P.I Chemical compound P.P.I RQTDRJMAUKHGHV-UHFFFAOYSA-N 0.000 description 3
- 241000209504 Poaceae Species 0.000 description 3
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- BFVNDLUCKHTAPA-UHFFFAOYSA-N 2-chloro-n-[2-methyl-6-(2-methylpropoxy)phenyl]acetamide Chemical compound CC(C)COC1=CC=CC(C)=C1NC(=O)CCl BFVNDLUCKHTAPA-UHFFFAOYSA-N 0.000 description 2
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- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
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- 239000002736 nonionic surfactant Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
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- 230000000704 physical effect Effects 0.000 description 1
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- 229920000570 polyether Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- AUPJTDWZPFFCCP-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCCN(C)CCS([O-])(=O)=O AUPJTDWZPFFCCP-GMFCBQQYSA-M 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000563 toxic property Toxicity 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 208000003982 trichinellosis Diseases 0.000 description 1
- 201000007588 trichinosis Diseases 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
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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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13369680A | 1980-03-25 | 1980-03-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL230201A1 PL230201A1 (ro) | 1981-11-13 |
| PL125385B1 true PL125385B1 (en) | 1983-05-31 |
Family
ID=22459887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1981230201A PL125385B1 (en) | 1980-03-25 | 1981-03-18 | Herbicide |
Country Status (33)
| Country | Link |
|---|---|
| JP (1) | JPS56145253A (ro) |
| AT (1) | AT376871B (ro) |
| AU (1) | AU537090B2 (ro) |
| BE (1) | BE887996A (ro) |
| BG (1) | BG36193A3 (ro) |
| BR (1) | BR8101598A (ro) |
| CA (1) | CA1221378A (ro) |
| CH (1) | CH644584A5 (ro) |
| CS (1) | CS226730B2 (ro) |
| DD (1) | DD158201A5 (ro) |
| DE (1) | DE3110451C2 (ro) |
| DK (1) | DK120881A (ro) |
| FR (1) | FR2479201B1 (ro) |
| GB (1) | GB2072176B (ro) |
| GR (1) | GR74140B (ro) |
| HU (1) | HU189498B (ro) |
| IL (1) | IL62412A (ro) |
| IT (1) | IT1144662B (ro) |
| KE (1) | KE3479A (ro) |
| LU (1) | LU83236A1 (ro) |
| MA (1) | MA19102A1 (ro) |
| MW (1) | MW1081A1 (ro) |
| MX (1) | MX6782E (ro) |
| NL (1) | NL8101323A (ro) |
| NZ (1) | NZ196543A (ro) |
| OA (1) | OA06770A (ro) |
| PH (1) | PH17172A (ro) |
| PL (1) | PL125385B1 (ro) |
| PT (1) | PT72679B (ro) |
| RO (2) | RO81729A (ro) |
| SE (1) | SE8101730L (ro) |
| SG (1) | SG84484G (ro) |
| ZA (1) | ZA811802B (ro) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56145252A (en) * | 1980-03-25 | 1981-11-11 | Monsanto Co | 2-haloacetanilide and its use |
| CH644587A5 (de) * | 1980-03-25 | 1984-08-15 | Monsanto Co | Herbizid wirksame 2-halogenacetanilide. |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3442945A (en) * | 1967-05-22 | 1969-05-06 | Monsanto Co | Phytotoxic alpha-halo-acetanilides |
| US3547620A (en) * | 1969-01-23 | 1970-12-15 | Monsanto Co | N-(oxamethyl)alpha-halo-acetanilide herbicides |
| US4258196A (en) * | 1978-04-17 | 1981-03-24 | Monsanto Company | Process for the production of tertiary 2-haloacetamides |
| JPS56145252A (en) * | 1980-03-25 | 1981-11-11 | Monsanto Co | 2-haloacetanilide and its use |
| CH644587A5 (de) * | 1980-03-25 | 1984-08-15 | Monsanto Co | Herbizid wirksame 2-halogenacetanilide. |
-
1981
- 1981-03-18 BR BR8101598A patent/BR8101598A/pt unknown
- 1981-03-18 RO RO81103732A patent/RO81729A/ro unknown
- 1981-03-18 PH PH25379A patent/PH17172A/en unknown
- 1981-03-18 RO RO110452A patent/RO85828B/ro unknown
- 1981-03-18 OA OA57356A patent/OA06770A/xx unknown
- 1981-03-18 AU AU68484/81A patent/AU537090B2/en not_active Ceased
- 1981-03-18 MA MA19308A patent/MA19102A1/fr unknown
- 1981-03-18 GB GB8108377A patent/GB2072176B/en not_active Expired
- 1981-03-18 IL IL62412A patent/IL62412A/xx unknown
- 1981-03-18 AT AT0125981A patent/AT376871B/de not_active IP Right Cessation
- 1981-03-18 SE SE8101730A patent/SE8101730L/ not_active Application Discontinuation
- 1981-03-18 IT IT20412/81A patent/IT1144662B/it active
- 1981-03-18 BG BG8151262A patent/BG36193A3/xx unknown
- 1981-03-18 GR GR64436A patent/GR74140B/el unknown
- 1981-03-18 DD DD81228416A patent/DD158201A5/de unknown
- 1981-03-18 CH CH184981A patent/CH644584A5/de not_active IP Right Cessation
- 1981-03-18 PL PL1981230201A patent/PL125385B1/pl unknown
- 1981-03-18 JP JP3807581A patent/JPS56145253A/ja active Pending
- 1981-03-18 PT PT72679A patent/PT72679B/pt unknown
- 1981-03-18 MX MX819354U patent/MX6782E/es unknown
- 1981-03-18 ZA ZA00811802A patent/ZA811802B/xx unknown
- 1981-03-18 CS CS811979A patent/CS226730B2/cs unknown
- 1981-03-18 NZ NZ196543A patent/NZ196543A/en unknown
- 1981-03-18 DE DE3110451A patent/DE3110451C2/de not_active Expired
- 1981-03-18 FR FR8105439A patent/FR2479201B1/fr not_active Expired
- 1981-03-18 BE BE0/204163A patent/BE887996A/fr not_active IP Right Cessation
- 1981-03-18 CA CA000373315A patent/CA1221378A/en not_active Expired
- 1981-03-18 LU LU83236A patent/LU83236A1/fr unknown
- 1981-03-18 NL NL8101323A patent/NL8101323A/nl not_active Application Discontinuation
- 1981-03-18 DK DK120881A patent/DK120881A/da not_active Application Discontinuation
- 1981-03-18 MW MW10/81A patent/MW1081A1/xx unknown
- 1981-03-18 HU HU81688A patent/HU189498B/hu unknown
-
1984
- 1984-11-21 KE KE3479A patent/KE3479A/xx unknown
- 1984-11-26 SG SG844/84A patent/SG84484G/en unknown
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