Weight | 375.468 g/mol |
---|---|
Formula | C24H25NO3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 6 |
Cyphenothrin (39515-40-7)
cyphenothrin, (1alpha(R*),3alpha)-(+-)-isomer · cyphenothrin, methyl ester-14C-labeled · cis-cyphenothrin
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- Quantum dots coated with molecularly imprinted polymer as fluorescence probe for detection of cyphenothrin. (Biosensors and Bioelectronics, 2015)
- Histopathological effects of cyphenothrin on the gills of Lebistes reticulatus. (Veterinary and Human Toxicology, 2000)
- Cyphenothrin phenothrin (Journal of Pesticide Science, 1984)
- The efficacy of a topically applied combination of cyphenothrin and pyriproxyfen against the southern African yellow dog tick, Haemaphysalis elliptica, and the cat flea, Ctenocephalides felis, on dogs (Journal of The South African Veterinary Association-tydskrif Van Die Suid-afrikaanse Veterinere Vereniging, 2010)
- Indoor thermal fogging application of pesguard FG 161, a mixture of d-tetramethrin and cyphenothrin, using portable sprayer against vector mosquitoes in the tropical environment. (Journal of The American Mosquito Control Association, 2001)
- Synthesis of an Aza-Analogue of Pyrethroid Cyphenothrin from (+)-3-Carene (Synthesis, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - cyphenothrin, (1alpha(R*),3alpha)-(+-)-isomer
- cyphenothrin, methyl ester-14C-labeled
- cis-cyphenothrin
- cyphenothrin, 1R-(1alpha(S*),3beta)-isomer
- cyphenothrin, 1R-(1alpha(S*),3alpha)-isomer
-
SMILESCC(=CC1C(C1(C)C)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C
-
InChIKeyFJDPATXIBIBRIM-UHFFFAOYSA-N
- Pubchem - Cyphenothrin
- Wikipedia - cyphenothrin
Cyphenothrin (Gokilaht) is a synthetic pyrethroid insecticide. It is effective against cockroaches that have developed resistance to organophosphorous and carbamate insecticides.
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Alternate Names
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Synthesis
Diphenyl oxide
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
phenoxyalcohol
(Dakin oxidation)
Similar Compounds
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(52315-07-8, 67375-30-8, 97955-44-7)
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(78-32-0, 1330-78-5)
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(126040-81-1, 95737-68-1)
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