IL22123A - 3-Chloro- and 5,3 -Dichloro- 4- (Mono- and dialkylamino) Anilides and herbicides containing them - Google Patents
3-Chloro- and 5,3 -Dichloro- 4- (Mono- and dialkylamino) Anilides and herbicides containing themInfo
- Publication number
- IL22123A IL22123A IL22123A IL2212364A IL22123A IL 22123 A IL22123 A IL 22123A IL 22123 A IL22123 A IL 22123A IL 2212364 A IL2212364 A IL 2212364A IL 22123 A IL22123 A IL 22123A
- Authority
- IL
- Israel
- Prior art keywords
- anilide
- composition according
- acid addition
- addition salt
- anilides
- Prior art date
Links
- 150000003931 anilides Chemical class 0.000 title claims description 55
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 title claims description 38
- 125000004663 dialkyl amino group Chemical group 0.000 title 1
- 239000000203 mixture Substances 0.000 claims description 37
- 239000002253 acid Substances 0.000 claims description 29
- 150000001875 compounds Chemical class 0.000 claims description 29
- 150000003839 salts Chemical class 0.000 claims description 27
- 241000196324 Embryophyta Species 0.000 claims description 24
- 230000002363 herbicidal effect Effects 0.000 claims description 21
- 239000007787 solid Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 15
- 238000002360 preparation method Methods 0.000 claims description 13
- 239000004009 herbicide Substances 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000460 chlorine Chemical group 0.000 claims description 9
- -1 isobutyryl Chemical group 0.000 claims description 9
- 229910052801 chlorine Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- ZTHRQJQJODGZHV-UHFFFAOYSA-N n-phenylpropanamide Chemical compound CCC(=O)NC1=CC=CC=C1 ZTHRQJQJODGZHV-UHFFFAOYSA-N 0.000 claims description 8
- 239000012141 concentrate Substances 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- IJSVVICYGLOZHA-UHFFFAOYSA-N 2-methyl-n-phenylprop-2-enamide Chemical compound CC(=C)C(=O)NC1=CC=CC=C1 IJSVVICYGLOZHA-UHFFFAOYSA-N 0.000 claims description 5
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- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
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- 239000006185 dispersion Substances 0.000 claims 3
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- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 1
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- 230000002035 prolonged effect Effects 0.000 description 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 235000009736 ragweed Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 235000005765 wild carrot Nutrition 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
- 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
- A01N37/22—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 the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic 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)
- 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 |
|---|---|---|---|
| US338596A US3281467A (en) | 1964-01-20 | 1964-01-20 | Herbicidal anilides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL22123A true IL22123A (en) | 1968-02-26 |
Family
ID=23325381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL22123A IL22123A (en) | 1964-01-20 | 1964-09-22 | 3-Chloro- and 5,3 -Dichloro- 4- (Mono- and dialkylamino) Anilides and herbicides containing them |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3281467A (en, 2012) |
| BE (1) | BE658554A (en, 2012) |
| BR (1) | BR6463257D0 (en, 2012) |
| CH (1) | CH447709A (en, 2012) |
| ES (1) | ES305220A1 (en, 2012) |
| GB (1) | GB1086339A (en, 2012) |
| IL (1) | IL22123A (en, 2012) |
| NL (1) | NL6500626A (en, 2012) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1473659A (en) * | 1973-11-27 | 1977-05-18 | Ici Ltd | Process for the monoacylation of aromatic diamines |
| DE2455212C2 (de) * | 1973-11-27 | 1984-09-13 | Imperial Chemical Industries Ltd., London | Verfahren zur Monoacylierung eines aromatischen Diamins |
| GB1500927A (en) * | 1975-12-10 | 1978-02-15 | Ici Ltd | Monoacylation of aromatic primary diamines |
| US4265658A (en) * | 1978-09-20 | 1981-05-05 | Stauffer Chemical Company | Novel cyclohexenone amino phenyl amides and their use as herbicides |
| DE3068646D1 (en) * | 1979-03-13 | 1984-08-30 | Ciba Geigy Ag | Substituted n-(p-aminophenyl)-n'-benzoyl ureas, process for their preparation, compositions containing them and their use as pesticides; alkenyl-substituted p-amino aniline derivatives |
| JPS6023357A (ja) * | 1983-07-19 | 1985-02-05 | Mitsui Toatsu Chem Inc | ２−メチル−４′−イソプロピル−２−ペンテノイルアニリドおよび選択性殺草剤 |
| DE10014141A1 (de) * | 2000-03-22 | 2001-10-11 | Jomaa Hassan | 2-Phenylendiaminderivate als Herbizide |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2226672A (en) * | 1938-01-28 | 1940-12-31 | Lloyd E Smith | Insecticide |
| US2357912A (en) * | 1940-03-14 | 1944-09-12 | Celanese Corp | Preparation of intermediates |
| US2368195A (en) * | 1941-09-15 | 1945-01-30 | Dow Chemical Co | Insecticidal compositions |
| US2552242A (en) * | 1948-03-06 | 1951-05-08 | Eastman Kodak Co | p-phenylenediamines containing n-alkylacetamido ethyl substituent |
| US2771466A (en) * | 1953-02-13 | 1956-11-20 | Eastman Kodak Co | 5-nitrothiazoleazo-n, n-disubstituted m-alkacylaminoaniline compounds |
| US2688637A (en) * | 1953-06-10 | 1954-09-07 | Dow Chemical Co | Nu-alkylcaproanilides |
| DE1005784B (de) * | 1956-02-03 | 1957-04-04 | Basf Ag | Unkrautbekaempfungsmittel |
| US3072471A (en) * | 1958-10-03 | 1963-01-08 | Us Rubber Co | Herbicidal and algaecidal composition and method |
| US3062636A (en) * | 1959-06-29 | 1962-11-06 | Velsicol Chemical Corp | Method and composition for controlling crabgrass |
-
1964
- 1964-01-20 US US338596A patent/US3281467A/en not_active Expired - Lifetime
- 1964-09-22 IL IL22123A patent/IL22123A/en unknown
- 1964-10-08 BR BR163257/64A patent/BR6463257D0/pt unknown
- 1964-10-23 ES ES0305220A patent/ES305220A1/es not_active Expired
-
1965
- 1965-01-05 GB GB450/65A patent/GB1086339A/en not_active Expired
- 1965-01-18 NL NL6500626A patent/NL6500626A/xx unknown
- 1965-01-20 BE BE658554D patent/BE658554A/xx unknown
- 1965-01-20 CH CH79565A patent/CH447709A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6500626A (en, 2012) | 1965-07-21 |
| BE658554A (en, 2012) | 1965-07-20 |
| ES305220A1 (es) | 1965-05-01 |
| US3281467A (en) | 1966-10-25 |
| GB1086339A (en) | 1967-10-11 |
| BR6463257D0 (pt) | 1973-08-07 |
| CH447709A (fr) | 1967-11-30 |
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