GB973353A - New substituted ureas and herbicidal compositions containing them - Google Patents
New substituted ureas and herbicidal compositions containing themInfo
- Publication number
- GB973353A GB973353A GB1102964A GB1102964A GB973353A GB 973353 A GB973353 A GB 973353A GB 1102964 A GB1102964 A GB 1102964A GB 1102964 A GB1102964 A GB 1102964A GB 973353 A GB973353 A GB 973353A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methoxy
- methylurea
- dichlorophenyl
- compositions
- specified
- 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
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/64—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups singly-bound to oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises urea derivatives of the formula <FORM:0973353/C1/1> in which n is 1, 2 or 3 and at least one of R1 and R2 is a methoxy group, the other denoting a hydrogen atom or a methyl or a methoxy group. Compounds in which R1 is a methoxy group may be prepared by reacting an appropriate phenylhydroxylamine with an appropriate methyl-substituted carbamyl chloride or with methyl isocyanate to yield a 3-phenyl-3-hydroxyurea which is then methylated, e.g. with dimethyl sulphate. Compounds in which R2 is a methoxy group may be prepared by reacting an appropriate phenylisocyanate with N-methoxymethylamine. Examples are given in which (1) 3-(3, 4-dichlorophenyl)-3-hydroxy-1, 1-dimethylurea is methylated with dimethyl sulphate to yield the 3-methoxy compound, and (2) 3-(p-chlorophenyl)-3-hydroxy-1, 1-dimethyl urea is similarly methylated. Other specified products are 3-(p-chlorophenyl)-3-methoxy-1-methylurea, 3-(3,4-dichlorophenyl)-3-methoxy-1-methylurea, 3-(2, 4, 5-trichlorophenyl)-3-methoxy-1-methylurea and 3-(3, 4-dichlorophenyl)-1, 3-dimethoxy-1-methylurea. The products are useful as herbicides (see Division A5).ALSO:As components of herbicidal compositions, use is made of urea derivatives of the formula <FORM:0973353/A5-A6/1> in which n is 1, 2 or 3 and at least one of R1 and R2 is a methoxy group, the other denoting a hydrogen atom or a methyl or a methoxy group. Specified products include 3 - (3,4 - dichlorophenyl) - 3 - methoxy - 1,1 - dimethylurea, 3 - (p-chlorophenyl) - 3 - methoxy - 1,1 - dimethyl urea, 3 - (p - chlorophenyl) - 3 - methoxy - 1 - methylurea, 3 - (3,4 - dichlorophenyl) - 3 - methoxy - 1 - methylurea, 3 - (2,4,5 - trichlorophenyl) - 3 - methoxy - 1 - methylurea and 3 - (3,4 - dichlorophenyl) - 1,3 - dimethoxy - 1 - methylurea. The products may be formulated as solid or liquid compositions with the addition of solid or liquid diluents, a number of which are specified. The compositions may also contain other herbicides, the specified additional herbicides including, among others, 3-(3,4-dichlorophenyl) - 1,1 - dimethylurea, pentachlorophenol and salts thereof, 2-methoxy-3,5,6-trichlorobenzoic acid and salts thereof, 2,6 - dichlorobenzonitrile, 2 - (2,4,5 - trichlorophenoxy)propionic acid and salts and esters thereof, trichloroacetic acid and its salts, N-phenylcarbamic acid isopropyl ester, N,N-dipropylthiol carbamic acid ethyl ester, 2-chloro - N,N - diallylacetamide, maleic hydrazide, 2 - chloro - 4 - ethylamino - 6 - isopropylamino - 5 - triazine, disodium monomethyl arsonate, sodium arsenite, sodium metaborate, sodium chlorate, ammonium sulphamate and 6,7 - dihydrodipyrido - (1,2A,21,11C) - pyrazinium dibromide. The compositions may also contain surface-active agents, a number of which are specified. Fertilizers, insecticides and fungicides may also be included in the compositions. The compositions may be used for the treatment of growing weeds or they may be applied to the soil in areas where a growth of weeds might otherwise have been expected. Examples of herbicidal compositions are given.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1102964A GB973353A (en) | 1960-10-31 | 1960-10-31 | New substituted ureas and herbicidal compositions containing them |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1102964A GB973353A (en) | 1960-10-31 | 1960-10-31 | New substituted ureas and herbicidal compositions containing them |
Publications (1)
Publication Number | Publication Date |
---|---|
GB973353A true GB973353A (en) | 1964-10-21 |
Family
ID=9978749
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1102964A Expired GB973353A (en) | 1960-10-31 | 1960-10-31 | New substituted ureas and herbicidal compositions containing them |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB973353A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3304408A1 (en) * | 1982-02-11 | 1983-11-24 | Albright & Wilson Ltd., Warley, West Midlands | Herbicidal preparation |
US8731598B2 (en) | 2007-02-02 | 2014-05-20 | Ubiquisys Limited | Access point power control |
-
1960
- 1960-10-31 GB GB1102964A patent/GB973353A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3304408A1 (en) * | 1982-02-11 | 1983-11-24 | Albright & Wilson Ltd., Warley, West Midlands | Herbicidal preparation |
US8731598B2 (en) | 2007-02-02 | 2014-05-20 | Ubiquisys Limited | Access point power control |
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