GB1315871A - Carbanilates thio-carbanilates and compositions containing them - Google Patents
Carbanilates thio-carbanilates and compositions containing themInfo
- Publication number
- GB1315871A GB1315871A GB1315871DA GB1315871A GB 1315871 A GB1315871 A GB 1315871A GB 1315871D A GB1315871D A GB 1315871DA GB 1315871 A GB1315871 A GB 1315871A
- Authority
- GB
- United Kingdom
- Prior art keywords
- maximum
- carbon atoms
- alkyl
- alkenyl
- halogen
- 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
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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
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)
Abstract
1315871 Pesticides containing carbanilates MONSANTO CO 19 May 1971 15810/71 Heading A5E [Also in Division C2] Pesticidal compositions comprise a diluent and as active ingredient a carbanilate of the general formula: in which Z<SP>1</SP> is selected from oxygen and sulfur; R<SP>1</SP> is selected from I. Hydrogen, II. R<SP>3</SP> - [B] n - wherein B is selected from carbonyl and oxygen; R<SP>3</SP> is selected from alkyl having a maximum of 18 carbon atoms; alkenyl having a maximum of 12 carbon atoms and alkynyl having at least 3 and a maximum of 12 carbon atoms; and n is 0 or 1; and III. R<SP>6</SP>O - [R<SP>5</SP>O] m - R<SP>4</SP> - wherein R<SP>4</SP> is alkylene which is substituted with an alkoxy group or an alkyl group or unsubstituted but which has not more than 4 carbon atoms in the main chain; R<SP>5</SP> is alkylene of not more than four carbon atoms; R<SP>6</SP> is selected from alkyl and alkenyl of not more than 6 carbon atoms; and m is 0 or 1; R<SP>2</SP> is selected from I. hydrogen, II. hydrocarbyl selected from alkyl having a maximum of 18 carbon atoms, alkenyl having a maximum of 12 carbon atoms, alkynyl having a maximum of 12 carbon atoms and haloalkyl having a maximum of atoms, and a maximum of 4 halogen atoms; III. R<SP>6</SP>O - [R<SP>5</SP>O] m - R<SP>4</SP> - wherein R<SP>4</SP>, R<SP>5</SP>, R<SP>6</SP> and m are as previously defined, except that R<SP>4</SP> may have up to 10 carbon atoms, IV. cycloalkyl, alkylcycloalkyl, cycloalkenyl, or alkylcycloalkenyl which may carry an alkoxy substituent having 3 to 7 ring carbon atoms and a maximum of 4 chain carbon atoms; V. phenyl and substituted phenyl having a maximum of two substituents said substituent being selected from the group consisting of halogen, alkyl having a maximum of four carbon atoms and -COOH; and VI. aralkyl of the formula: wherein R<SP>7</SP> is selected from hydrogen, alkyl having a maximum of 4 carbon atoms, alkenyl having a maximum of 3 carbon atoms and haloalkyl having a maximum of 4 carbon atoms and a maximum of three halogen atoms; R<SP>8</SP> is selected from hydrogen, alkyl having a maximum of 4 carbon atoms and haloalkyl having a maximum of 4 carbon atoms and a maximum of 3 halogen atoms; R<SP>9</SP> is independently selected from the group consisting of alkyl having a maximum of 4 carbon atoms, alkoxy having a maximum of 2 carbon atoms, -COOH, and halogen; p is zero one or two; and q is zero one or two; or diphenylmethyl VII arakenyl other than as defined in VI and A is wherein Z<SP>5</SP> and Z<SP>6</SP> are each independently selected from oxygen and sulfur; R<SP>20</SP> is selected from hydrogen, alkyl having a maximum of 6 carbon atoms and alkenyl having a maximum of 6 carbon atoms; and R<SP>21</SP> is selected from alkyl having a maximum of 8 carbon atoms, alkenyl having a maximum of 6 carbon atoms; cycloalkyl having from 3 to 7 ring carbon atoms; cyclohexenyl, phenyl, substituted phenyl having a maximum of two substituents said substituents being selected from the group consisting of halogen, nitro and alkyl having a maximum of 4 carbon atoms, the group and the group wherein R<SP>12</SP> and R<SP>13</SP> are each independently selected from hydrogen, alkyl having a maximum of 4 carbon atoms, alkenyl having a maximum of 3 carbon atoms, chloroalkyl having a maximum of 3 carbon atoms and a maximum of 3 halogen atoms, chloroalkenyl having a maximum of 3 carbon atoms and 3 halogen atoms, provided that only one of R<SP>12</SP> and R<SP>13</SP> can be alkenyl or chloroalkenyl; R<SP>14</SP> is selected from halogen, alkyl having a maximum of 4 carbon atoms, nitro, alkoxy having a maximum of 3 carbon atoms, R<SP>15</SP> is selected from alkyl and alkenyl each having a maximum of 4 carbon atoms and hydrogen, provided that R<SP>15</SP> is other than alkenyl where either R<SP>12</SP> or R<SP>13</SP> is alkenyl, and r is zero one or two. There may also be incorporated, for example fertilisers, phytotoxicants, plant growth regulants, pesticides such as ammonium nitrate, urea, potash, and super-phosphate, compost, manure, humus, and sand triazines, ureas, carbamates, acetamides, acetanilides, aracils, acetic acids, phenols, thiols, thiolcarbamates, triazoles, benzoic acids, and nitriles, many examples being specified.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1581071 | 1971-05-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1315871A true GB1315871A (en) | 1973-05-02 |
Family
ID=10065895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1315871D Expired GB1315871A (en) | 1971-05-19 | 1971-05-19 | Carbanilates thio-carbanilates and compositions containing them |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1315871A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0021324A1 (en) * | 1979-06-28 | 1981-01-07 | BASF Aktiengesellschaft | m-Anilido urethanes and herbicidal compositions which contain them |
EP0153533A1 (en) * | 1984-01-06 | 1985-09-04 | Becton Dickinson and Company | Rigid coupling compounds |
EP0448237A2 (en) * | 1990-03-21 | 1991-09-25 | Texaco Chemical Company | Aliphatic polyamines from polynitro compounds |
-
1971
- 1971-05-19 GB GB1315871D patent/GB1315871A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0021324A1 (en) * | 1979-06-28 | 1981-01-07 | BASF Aktiengesellschaft | m-Anilido urethanes and herbicidal compositions which contain them |
EP0153533A1 (en) * | 1984-01-06 | 1985-09-04 | Becton Dickinson and Company | Rigid coupling compounds |
EP0448237A2 (en) * | 1990-03-21 | 1991-09-25 | Texaco Chemical Company | Aliphatic polyamines from polynitro compounds |
EP0448237A3 (en) * | 1990-03-21 | 1993-01-20 | Texaco Chemical Company | Aliphatic polyamines from polynitro compounds |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |