DD202088A5 - Herbizides mittel - Google Patents
Herbizides mittel Download PDFInfo
- Publication number
- DD202088A5 DD202088A5 DD82239384A DD23938482A DD202088A5 DD 202088 A5 DD202088 A5 DD 202088A5 DD 82239384 A DD82239384 A DD 82239384A DD 23938482 A DD23938482 A DD 23938482A DD 202088 A5 DD202088 A5 DD 202088A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- active ingredient
- carbon atoms
- alkyl group
- group
- general formula
- Prior art date
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- 239000004009 herbicide Substances 0.000 title claims description 8
- 239000004480 active ingredient Substances 0.000 claims abstract description 46
- 239000000203 mixture Substances 0.000 claims abstract description 28
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000005599 alkyl carboxylate group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract description 42
- 150000001875 compounds Chemical class 0.000 abstract description 36
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 15
- 235000010469 Glycine max Nutrition 0.000 abstract description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 9
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- 239000002253 acid Substances 0.000 abstract description 9
- -1 2-chloro-4- (trifluoromethyl) phenoxy Chemical group 0.000 abstract description 7
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- 238000001816 cooling Methods 0.000 abstract description 2
- 229940081974 saccharin Drugs 0.000 abstract description 2
- 235000019204 saccharin Nutrition 0.000 abstract description 2
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 abstract description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 2
- MAGRFJCHFXFWOS-UHFFFAOYSA-N 2-(benzoylsulfamoyl)benzoic acid Chemical compound C(C1=CC=CC=C1)(=O)NS(=O)(=O)C1=C(C=CC=C1)C(=O)O MAGRFJCHFXFWOS-UHFFFAOYSA-N 0.000 abstract 1
- KGPHNHSAYAXSOW-UHFFFAOYSA-N 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride Chemical compound C1=C(C(Cl)=O)C([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1Cl KGPHNHSAYAXSOW-UHFFFAOYSA-N 0.000 abstract 1
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- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
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- 229960000278 theophylline Drugs 0.000 description 3
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 3
- PKRSYEPBQPFNRB-UHFFFAOYSA-N 2-phenoxybenzoic acid Chemical class OC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PKRSYEPBQPFNRB-UHFFFAOYSA-N 0.000 description 2
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- 239000013558 reference substance Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 150000004760 silicates Chemical class 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
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A01N41/06—Sulfonic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/259,336 US4447634A (en) | 1981-04-30 | 1981-04-30 | Herbicidal arylsulfonamide derivatives of phenoxybenzoic acids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD202088A5 true DD202088A5 (de) | 1983-08-31 |
Family
ID=22984519
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD82239384A DD202088A5 (de) | 1981-04-30 | 1982-04-28 | Herbizides mittel |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4447634A (cs) |
| JP (1) | JPS57185258A (cs) |
| KR (1) | KR830010061A (cs) |
| AU (1) | AU8306282A (cs) |
| BE (1) | BE893028A (cs) |
| BR (1) | BR8202523A (cs) |
| CS (1) | CS228925B2 (cs) |
| DD (1) | DD202088A5 (cs) |
| DE (1) | DE3215991A1 (cs) |
| DK (1) | DK191482A (cs) |
| ES (1) | ES8306717A1 (cs) |
| GB (1) | GB2098207A (cs) |
| GR (1) | GR75424B (cs) |
| IL (1) | IL65628A0 (cs) |
| IT (1) | IT1153498B (cs) |
| LU (1) | LU84116A1 (cs) |
| MA (1) | MA19459A1 (cs) |
| NL (1) | NL8201783A (cs) |
| OA (1) | OA07087A (cs) |
| PL (1) | PL236203A1 (cs) |
| PT (1) | PT74826B (cs) |
| RO (1) | RO83848B (cs) |
| SE (1) | SE8202423L (cs) |
| TR (1) | TR21156A (cs) |
| ZA (1) | ZA822910B (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH658453A5 (fr) * | 1982-12-17 | 1986-11-14 | Rhone Poulenc Agrochimie | Procede pour la preparation d'acides aryloxybenzoiques a groupe sulfonamide. |
| DE4427995A1 (de) * | 1994-08-08 | 1996-02-15 | Basf Ag | Saccharinderivate |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3317540A (en) * | 1964-07-30 | 1967-05-02 | Milimaster Onyx Corp | Microbiocidal quaternary ammonium aromatic sulfonamides |
| US3622626A (en) * | 1968-12-18 | 1971-11-23 | Minnesota Mining & Mfg | N-acylated perfluoroalkanesulfonamides |
| US3641114A (en) * | 1969-06-03 | 1972-02-08 | American Home Prod | 2-lower alkanoyloxy-n-sulfonylbenzamides |
| US3663615A (en) * | 1970-03-02 | 1972-05-16 | Merck & Co Inc | Nuclear sulfamoyl n-organosulfonyl benzamides |
| US3906024A (en) * | 1971-02-24 | 1975-09-16 | Minnesota Mining & Mfg | Perfluoroalkanesulfonamidoaryl compounds |
| US4063929A (en) * | 1973-02-12 | 1977-12-20 | Rohm And Haas Company | Herbicidal 4-trifluoromethyl-4'nitrodiphenyl ethers |
| GR65995B (cs) * | 1978-01-19 | 1981-01-13 | Ici Ltd |
-
1981
- 1981-04-30 US US06/259,336 patent/US4447634A/en not_active Expired - Fee Related
-
1982
- 1982-04-19 SE SE8202423A patent/SE8202423L/xx not_active Application Discontinuation
- 1982-04-22 MA MA19664A patent/MA19459A1/fr unknown
- 1982-04-26 RO RO107369A patent/RO83848B/ro unknown
- 1982-04-27 IL IL65628A patent/IL65628A0/xx unknown
- 1982-04-27 JP JP57071126A patent/JPS57185258A/ja active Pending
- 1982-04-28 PL PL23620382A patent/PL236203A1/xx unknown
- 1982-04-28 DD DD82239384A patent/DD202088A5/de unknown
- 1982-04-28 LU LU84116A patent/LU84116A1/fr unknown
- 1982-04-28 AU AU83062/82A patent/AU8306282A/en not_active Abandoned
- 1982-04-28 ZA ZA822910A patent/ZA822910B/xx unknown
- 1982-04-28 GB GB8212295A patent/GB2098207A/en not_active Withdrawn
- 1982-04-29 GR GR68023A patent/GR75424B/el unknown
- 1982-04-29 ES ES511809A patent/ES8306717A1/es not_active Expired
- 1982-04-29 DE DE19823215991 patent/DE3215991A1/de not_active Withdrawn
- 1982-04-29 BE BE0/207970A patent/BE893028A/fr not_active IP Right Cessation
- 1982-04-29 NL NL8201783A patent/NL8201783A/nl not_active Application Discontinuation
- 1982-04-29 TR TR21156A patent/TR21156A/xx unknown
- 1982-04-29 DK DK191482A patent/DK191482A/da not_active Application Discontinuation
- 1982-04-29 PT PT74826A patent/PT74826B/pt unknown
- 1982-04-30 BR BR8202523A patent/BR8202523A/pt unknown
- 1982-04-30 OA OA57673A patent/OA07087A/xx unknown
- 1982-04-30 CS CS823126A patent/CS228925B2/cs unknown
- 1982-04-30 IT IT21031/82A patent/IT1153498B/it active
- 1982-04-30 KR KR1019820001911A patent/KR830010061A/ko not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US4447634A (en) | 1984-05-08 |
| ZA822910B (en) | 1983-12-28 |
| DE3215991A1 (de) | 1982-11-18 |
| CS228925B2 (en) | 1984-05-14 |
| PT74826B (fr) | 1985-01-07 |
| MA19459A1 (fr) | 1982-12-31 |
| RO83848A (ro) | 1984-04-12 |
| KR830010061A (ko) | 1983-12-24 |
| BE893028A (fr) | 1982-10-29 |
| OA07087A (fr) | 1984-01-31 |
| DK191482A (da) | 1982-10-31 |
| RO83848B (ro) | 1984-05-30 |
| SE8202423L (sv) | 1982-10-31 |
| GR75424B (cs) | 1984-07-17 |
| IT1153498B (it) | 1987-01-14 |
| BR8202523A (pt) | 1983-04-19 |
| GB2098207A (en) | 1982-11-17 |
| NL8201783A (nl) | 1982-11-16 |
| JPS57185258A (en) | 1982-11-15 |
| TR21156A (tr) | 1983-11-28 |
| IL65628A0 (en) | 1982-07-30 |
| PT74826A (fr) | 1982-05-01 |
| IT8221031A0 (it) | 1982-04-30 |
| PL236203A1 (en) | 1983-02-28 |
| LU84116A1 (fr) | 1984-03-02 |
| AU8306282A (en) | 1982-11-04 |
| ES511809A0 (es) | 1983-06-01 |
| ES8306717A1 (es) | 1983-06-01 |
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