| Identification | Back Directory | [Name]
ESFENVALERATE FREE ACID METABOLITE | [CAS]
55332-38-2 | [Synonyms]
S-2-(4-chlorophenyl)-3-methylbutyricacid
(S)-2-(4-Chlorophenyl)-3-methylbutanoicaci
Benzeneacetic acid, 4-chloro-α-(1-methylethyl)-, (αS)-
Benzeneacetic acid, 4-chloro-a-(1-methylethyl)-, (aS)-
Esfenvalerate free acid metabolite, 10 μg /μL in cyclohexane
Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-, (alphaS)- | [Molecular Formula]
C11H13ClO2 | [MDL Number]
MFCD04112625 | [MOL File]
55332-38-2.mol | [Molecular Weight]
212.68 |
| Chemical Properties | Back Directory | [Melting point ]
89-91 °C | [Boiling point ]
318.7±17.0 °C(Predicted) | [density ]
1.184±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
4.13±0.10(Predicted) | [CAS DataBase Reference]
55332-38-2 |
| Hazard Information | Back Directory | [Chemical Properties]
S-2-(4-chlorophenyl)-3-methylbutanoic acid is a white solid, mp106～107℃, insoluble in water, soluble in organic solvents such as toluene and benzene. | [Uses]
S-2-(4-chlorophenyl)-3-methylbutyric acid is an intermediate of S-fenvalerate (also known as S,S-fenvalerate, esfenvalerate), which can be used in related chemical in experimental research. | [Synthesis]
S-2-(4-chlorophenyl)-3-methylbutyric acid can be used with racemic 2-(4-chlorophenyl)-3-methylbutyric acid (referred to as butyric acid) with α-methylbenzylamine It can be obtained by splitting, but it is generally prepared by the dominant crystallization separation method in industry,. |
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SynAsst Chemical.
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