GB994481A - Substituted n-phenyl-n-alkoxy-n-alkyl-ureas and a process for their manufacture - Google Patents
Substituted n-phenyl-n-alkoxy-n-alkyl-ureas and a process for their manufactureInfo
- Publication number
- GB994481A GB994481A GB2934061A GB2934061A GB994481A GB 994481 A GB994481 A GB 994481A GB 2934061 A GB2934061 A GB 2934061A GB 2934061 A GB2934061 A GB 2934061A GB 994481 A GB994481 A GB 994481A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- formula
- methoxyurea
- phenyl
- compounds
- 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
- 238000000034 method Methods 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 8
- -1 alkyl radical Chemical group 0.000 abstract 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 230000000895 acaricidal effect Effects 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 230000002363 herbicidal effect Effects 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 241000219321 Caryophyllaceae Species 0.000 abstract 1
- 235000002845 Dianthus plumarius Nutrition 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 244000046052 Phaseolus vulgaris Species 0.000 abstract 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 abstract 1
- 240000004713 Pisum sativum Species 0.000 abstract 1
- 235000010582 Pisum sativum Nutrition 0.000 abstract 1
- 241001454295 Tetranychidae Species 0.000 abstract 1
- 240000008042 Zea mays Species 0.000 abstract 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 abstract 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 239000002168 alkylating agent Substances 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000007900 aqueous suspension Substances 0.000 abstract 1
- RDEAKCXMQCTSEB-UHFFFAOYSA-N butoxyurea Chemical compound CCCCONC(N)=O RDEAKCXMQCTSEB-UHFFFAOYSA-N 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 235000005822 corn Nutrition 0.000 abstract 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- 150000002513 isocyanates Chemical class 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- WCVVIGQKJZLJDB-UHFFFAOYSA-N o-butylhydroxylamine Chemical compound CCCCON WCVVIGQKJZLJDB-UHFFFAOYSA-N 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000003755 preservative agent Substances 0.000 abstract 1
- 230000002335 preservative effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF31874A DE1189980B (de) | 1960-08-13 | 1960-08-13 | Verfahren zur Herstellung von Harnstoffderivaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB994481A true GB994481A (en) | 1965-06-10 |
Family
ID=7094397
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2934061A Expired GB994481A (en) | 1960-08-13 | 1961-08-14 | Substituted n-phenyl-n-alkoxy-n-alkyl-ureas and a process for their manufacture |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE607204A (enrdf_load_stackoverflow) |
| DE (1) | DE1189980B (enrdf_load_stackoverflow) |
| FR (2) | FR1220593A (enrdf_load_stackoverflow) |
| GB (1) | GB994481A (enrdf_load_stackoverflow) |
| NL (1) | NL267999A (enrdf_load_stackoverflow) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1028986B (de) * | 1956-01-17 | 1958-04-30 | Hoechst Ag | Verfahren zur Herstellung von neuen Harnstoffderivaten |
| BE573402A (enrdf_load_stackoverflow) * | 1957-12-05 | |||
| DE1076117B (de) * | 1958-04-17 | 1960-02-25 | Hoechst Ag | Verfahren zur Herstellung von N-Chlorphenyl-N'-alkoxy-N'-alkylharnstoffen |
-
1959
- 1959-04-16 FR FR792313A patent/FR1220593A/fr not_active Expired
-
1960
- 1960-08-13 DE DEF31874A patent/DE1189980B/de active Pending
-
1961
- 1961-08-08 NL NL267999D patent/NL267999A/xx unknown
- 1961-08-11 FR FR870796A patent/FR83353E/fr not_active Expired
- 1961-08-14 BE BE607204D patent/BE607204A/xx unknown
- 1961-08-14 GB GB2934061A patent/GB994481A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR83353E (fr) | 1964-07-31 |
| FR1220593A (fr) | 1960-05-25 |
| NL267999A (enrdf_load_stackoverflow) | 1964-01-27 |
| DE1189980B (de) | 1965-04-01 |
| BE607204A (enrdf_load_stackoverflow) | 1962-02-14 |
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