GB912356A - Improvements in or relating to 2-chloro-5-isopropylphenyl n-methylcarbamate - Google Patents
Improvements in or relating to 2-chloro-5-isopropylphenyl n-methylcarbamateInfo
- Publication number
- GB912356A GB912356A GB2907561A GB2907561A GB912356A GB 912356 A GB912356 A GB 912356A GB 2907561 A GB2907561 A GB 2907561A GB 2907561 A GB2907561 A GB 2907561A GB 912356 A GB912356 A GB 912356A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloro
- isopropylphenyl
- isopropylphenol
- methylcarbamate
- phosgene
- 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
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises the compounds 2-, 4- and 6-chloro-3-isopropylphenyl-N-methylcarbamate and a process for their preparation by reacting monochloro-m-isopropylphenol with methyl isocyanate or N-methylcarbamyl chloride, or with phosgene and subsequently methylamine. In the example a mixture of 2-, 4- and 6-chloro-3-isopropylphenol, obtained by chlorination of m-isopropylphenol with Cl2 gas, was reacted with phosgene giving chloro-m-isopropylphenyl chlorocarbonate which was subsequently reacted with methylamine. The individual isomers were separated by distillation.ALSO:An insecticidal composition comprises 6-chloro - 3 - isopropylphenyl - N - methylcarbamate (optionally admixed with the 2- and 4-chloro isomers) and an inert carrier. The composition may take the form of wettable powders, aqueous emulsions, dusts of clays mixed with the active ingredient or deodorized kerosene solutions thereof. Other toxicants such as toxaphene, DDT, thanite, chlordane, rotenone or pyrethrum may be present. Aqueous dispersions containing a surface-active agent are preferred (many of such agents being specified), but dispersions in e.g. alcohols, pine oil, hydrocarbon solvents and difluorodichloromethane-including aerosols in the latter-are also mentioned.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4911760A | 1960-08-12 | 1960-08-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB912356A true GB912356A (en) | 1962-12-05 |
Family
ID=21958134
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2907561A Expired GB912356A (en) | 1960-08-12 | 1961-08-11 | Improvements in or relating to 2-chloro-5-isopropylphenyl n-methylcarbamate |
Country Status (3)
Country | Link |
---|---|
FR (1) | FR1301496A (en) |
GB (1) | GB912356A (en) |
NL (1) | NL268094A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3402247A (en) * | 1966-04-04 | 1968-09-17 | Hercules Inc | 2-chloro-5-isopropylphenyl n-chloroacetyl-n-methylcarbamates and their use as pesticides |
-
0
- NL NL268094D patent/NL268094A/xx unknown
-
1961
- 1961-08-11 GB GB2907561A patent/GB912356A/en not_active Expired
- 1961-08-11 FR FR41801A patent/FR1301496A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3402247A (en) * | 1966-04-04 | 1968-09-17 | Hercules Inc | 2-chloro-5-isopropylphenyl n-chloroacetyl-n-methylcarbamates and their use as pesticides |
Also Published As
Publication number | Publication date |
---|---|
NL268094A (en) | |
FR1301496A (en) | 1962-08-17 |
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