GB895952A - Molluscicides - Google Patents
MolluscicidesInfo
- Publication number
- GB895952A GB895952A GB567460A GB567460A GB895952A GB 895952 A GB895952 A GB 895952A GB 567460 A GB567460 A GB 567460A GB 567460 A GB567460 A GB 567460A GB 895952 A GB895952 A GB 895952A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carboxylic acid
- ester
- phenyl
- semicarbazide
- hydrazine
- 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
- 230000002013 molluscicidal effect Effects 0.000 title abstract 2
- 239000003750 molluscacide Substances 0.000 title 1
- 239000004480 active ingredient Substances 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- MLQSMEOEJDBQGD-UHFFFAOYSA-N (4-chlorophenyl) N-anilino-N-phenylcarbamate Chemical compound ClC1=CC=C(C=C1)OC(=O)N(NC1=CC=CC=C1)C1=CC=CC=C1 MLQSMEOEJDBQGD-UHFFFAOYSA-N 0.000 abstract 1
- LBCBAVSDWDSWJE-UHFFFAOYSA-N 1,1-dimethyl-3-(3-methylanilino)-3-(3-methylphenyl)urea Chemical compound CN(C(=O)N(NC1=CC(=CC=C1)C)C1=CC(=CC=C1)C)C LBCBAVSDWDSWJE-UHFFFAOYSA-N 0.000 abstract 1
- XJOJXKFVLQMIJI-UHFFFAOYSA-N 1-(4-chloroanilino)-1-(4-chlorophenyl)-3-phenylurea Chemical compound ClC1=CC=C(C=C1)N(NC1=CC=C(C=C1)Cl)C(=O)NC1=CC=CC=C1 XJOJXKFVLQMIJI-UHFFFAOYSA-N 0.000 abstract 1
- CRMMYYOMBWPPTD-UHFFFAOYSA-N 1-amino-3-butyl-1-(3-methoxyphenyl)urea Chemical compound COC=1C=C(C=CC1)N(N)C(=O)NCCCC CRMMYYOMBWPPTD-UHFFFAOYSA-N 0.000 abstract 1
- WZWBPPGTRCXNID-UHFFFAOYSA-N 1-amino-3-butyl-1-(4-chlorophenyl)urea Chemical compound ClC1=CC=C(C=C1)N(N)C(=O)NCCCC WZWBPPGTRCXNID-UHFFFAOYSA-N 0.000 abstract 1
- QCGVRVVXKDLXCE-UHFFFAOYSA-N 1-amino-3-butyl-1-(4-nitrophenyl)urea Chemical compound [N+](=O)([O-])C1=CC=C(C=C1)N(N)C(=O)NCCCC QCGVRVVXKDLXCE-UHFFFAOYSA-N 0.000 abstract 1
- SQVZCWUQTJDFTR-UHFFFAOYSA-N 1-amino-3-ethyl-1-(2-methylphenyl)urea Chemical compound CC1=C(C=CC=C1)N(N)C(=O)NCC SQVZCWUQTJDFTR-UHFFFAOYSA-N 0.000 abstract 1
- ZXTHWIZHGLNEPG-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1 ZXTHWIZHGLNEPG-UHFFFAOYSA-N 0.000 abstract 1
- XDTXSAFYHXCSHL-UHFFFAOYSA-N C1(CCCCC1)OC(=O)N(NC1=CC(=CC=C1)Cl)C1=CC(=CC=C1)Cl Chemical compound C1(CCCCC1)OC(=O)N(NC1=CC(=CC=C1)Cl)C1=CC(=CC=C1)Cl XDTXSAFYHXCSHL-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- HJLJEHJDTKXCAF-UHFFFAOYSA-N butyl N-anilino-N-phenylcarbamate Chemical compound C(CCC)OC(=O)N(NC1=CC=CC=C1)C1=CC=CC=C1 HJLJEHJDTKXCAF-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- JASQPPGOALJCSP-UHFFFAOYSA-N phenyl N-(4-methoxyanilino)-N-(4-methoxyphenyl)carbamate Chemical compound C1(=CC=CC=C1)OC(=O)N(NC1=CC=C(C=C1)OC)C1=CC=C(C=C1)OC JASQPPGOALJCSP-UHFFFAOYSA-N 0.000 abstract 1
- MNSIUPWZWUYEOX-UHFFFAOYSA-N phenyl N-anilino-N-phenylcarbamate Chemical compound C1(=CC=CC=C1)OC(=O)N(NC1=CC=CC=C1)C1=CC=CC=C1 MNSIUPWZWUYEOX-UHFFFAOYSA-N 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE587203D BE587203A (en)) | 1960-02-17 | ||
| DEF25380A DE1081713B (de) | 1958-03-31 | 1958-03-31 | Schneckenbekaempfungsmittel |
| FR817243A FR1247133A (fr) | 1960-02-01 | 1960-02-01 | Procédé pour combattre les limaces |
| US8929A US3058880A (en) | 1960-02-16 | 1960-02-16 | Process for combating snails |
| GB567460A GB895952A (en) | 1960-02-17 | 1960-02-17 | Molluscicides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB567460A GB895952A (en) | 1960-02-17 | 1960-02-17 | Molluscicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB895952A true GB895952A (en) | 1962-05-09 |
Family
ID=9800515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB567460A Expired GB895952A (en) | 1958-03-31 | 1960-02-17 | Molluscicides |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE587203A (en)) |
| GB (1) | GB895952A (en)) |
-
0
- BE BE587203D patent/BE587203A/xx unknown
-
1960
- 1960-02-17 GB GB567460A patent/GB895952A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE587203A (en)) |
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