GB1465568A - Cyclopropane carboxylic acid derivatives - Google Patents
Cyclopropane carboxylic acid derivativesInfo
- Publication number
- GB1465568A GB1465568A GB4565374A GB4565374A GB1465568A GB 1465568 A GB1465568 A GB 1465568A GB 4565374 A GB4565374 A GB 4565374A GB 4565374 A GB4565374 A GB 4565374A GB 1465568 A GB1465568 A GB 1465568A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- formula
- ethyl
- alkyl
- substituted
- 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
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 title abstract 3
- -1 alkyl radical Chemical class 0.000 abstract 13
- 150000001875 compounds Chemical class 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 5
- 229910052783 alkali metal Inorganic materials 0.000 abstract 4
- 150000001340 alkali metals Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- DNHLVEFLSIKNPI-UHFFFAOYSA-N 1-[ethyl(triphenyl)-lambda5-phosphanyl]propan-2-one Chemical compound C(C)P(C1=CC=CC=C1)(C1=CC=CC=C1)(C1=CC=CC=C1)CC(=O)C DNHLVEFLSIKNPI-UHFFFAOYSA-N 0.000 abstract 2
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 abstract 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- PTQGFDXPHNRDCV-UHFFFAOYSA-N 3-formyl-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=O)C1C(O)=O PTQGFDXPHNRDCV-UHFFFAOYSA-N 0.000 abstract 1
- UZTZKICRSWXRFQ-UHFFFAOYSA-N 3a,4,5,6-tetrahydroisoindole-1,3-dione Chemical compound C1CCC2C(=O)NC(=O)C2=C1 UZTZKICRSWXRFQ-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 abstract 1
- APTGPWJUOYMUCE-UHFFFAOYSA-N S-Ethyl thioacetate Chemical compound CCSC(C)=O APTGPWJUOYMUCE-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000005840 aryl radicals Chemical class 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- MPNQDJZRGAOBPW-UHFFFAOYSA-M triphenyl(propyl)phosphanium;iodide Chemical compound [I-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCC)C1=CC=CC=C1 MPNQDJZRGAOBPW-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
- C07D209/49—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide and having in the molecule an acyl radical containing a saturated three-membered ring, e.g. chrysanthemumic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/535—Organo-phosphoranes
- C07F9/5352—Phosphoranes containing the structure P=C-
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7337540A FR2248264B1 (cg-RX-API-DMAC7.html) | 1973-10-22 | 1973-10-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1465568A true GB1465568A (en) | 1977-02-23 |
Family
ID=9126733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4565374A Expired GB1465568A (en) | 1973-10-22 | 1974-10-22 | Cyclopropane carboxylic acid derivatives |
Country Status (15)
| Country | Link |
|---|---|
| JP (1) | JPS5070342A (cg-RX-API-DMAC7.html) |
| BE (1) | BE821299A (cg-RX-API-DMAC7.html) |
| CA (1) | CA1053245A (cg-RX-API-DMAC7.html) |
| CH (1) | CH602553A5 (cg-RX-API-DMAC7.html) |
| DE (1) | DE2449643A1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK549774A (cg-RX-API-DMAC7.html) |
| FR (1) | FR2248264B1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1465568A (cg-RX-API-DMAC7.html) |
| HU (1) | HU172070B (cg-RX-API-DMAC7.html) |
| IE (1) | IE41764B1 (cg-RX-API-DMAC7.html) |
| IL (1) | IL45878A (cg-RX-API-DMAC7.html) |
| IT (1) | IT1059698B (cg-RX-API-DMAC7.html) |
| LU (1) | LU71148A1 (cg-RX-API-DMAC7.html) |
| NL (1) | NL7413780A (cg-RX-API-DMAC7.html) |
| SE (1) | SE419214B (cg-RX-API-DMAC7.html) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2730515A1 (de) * | 1977-07-06 | 1979-01-18 | Bayer Ag | Substituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
-
1973
- 1973-10-22 FR FR7337540A patent/FR2248264B1/fr not_active Expired
-
1974
- 1974-10-14 SE SE7412895A patent/SE419214B/xx unknown
- 1974-10-18 DE DE19742449643 patent/DE2449643A1/de not_active Ceased
- 1974-10-18 IL IL45878A patent/IL45878A/xx unknown
- 1974-10-21 CH CH1405974A patent/CH602553A5/xx not_active IP Right Cessation
- 1974-10-21 IT IT53641/74A patent/IT1059698B/it active
- 1974-10-21 DK DK549774A patent/DK549774A/da unknown
- 1974-10-21 BE BE149726A patent/BE821299A/xx not_active IP Right Cessation
- 1974-10-21 NL NL7413780A patent/NL7413780A/xx not_active Application Discontinuation
- 1974-10-21 LU LU71148A patent/LU71148A1/xx unknown
- 1974-10-21 CA CA211,900A patent/CA1053245A/fr not_active Expired
- 1974-10-22 GB GB4565374A patent/GB1465568A/en not_active Expired
- 1974-10-22 JP JP49121088A patent/JPS5070342A/ja active Pending
- 1974-10-22 HU HU74RO00000805A patent/HU172070B/hu unknown
- 1974-10-22 IE IE2174/74A patent/IE41764B1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH602553A5 (cg-RX-API-DMAC7.html) | 1978-07-31 |
| NL7413780A (nl) | 1975-04-24 |
| FR2248264A1 (cg-RX-API-DMAC7.html) | 1975-05-16 |
| IT1059698B (it) | 1982-06-21 |
| SE419214B (sv) | 1981-07-20 |
| FR2248264B1 (cg-RX-API-DMAC7.html) | 1977-05-27 |
| IE41764B1 (en) | 1980-03-26 |
| SE7412895L (cg-RX-API-DMAC7.html) | 1975-04-23 |
| CA1053245A (fr) | 1979-04-24 |
| DE2449643A1 (de) | 1975-04-30 |
| DK549774A (cg-RX-API-DMAC7.html) | 1975-07-07 |
| IL45878A0 (en) | 1974-12-31 |
| HU172070B (hu) | 1978-05-28 |
| IL45878A (en) | 1979-10-31 |
| LU71148A1 (cg-RX-API-DMAC7.html) | 1975-06-24 |
| IE41764L (en) | 1975-04-22 |
| JPS5070342A (cg-RX-API-DMAC7.html) | 1975-06-11 |
| BE821299A (fr) | 1975-04-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |