Cas 82095-85-0,(1R,3S)-3-(2-Chloro-ethyl)-2,2-dimethyl-cyclopropanecarboxylic acid 2-isopropyl-5-methyl-cyclohexyl ester

82095-85-0

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Basic information

Product Name: (1R,3S)-3-(2-Chloro-ethyl)-2,2-dimethyl-cyclopropanecarboxylic acid 2-isopropyl-5-methyl-cyclohexyl ester
Synonyms:
CAS NO:82095-85-0
Molecular Formula:
Molecular Weight: 314.896
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1R,3S)-3-(2-Chloro-ethyl)-2,2-dimethyl-cyclopropanecarboxylic acid 2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3S)-3-(2-Chloro-ethyl)-2,2-dimethyl-cyclopropanecarboxylic acid 2-isopropyl-5-methyl-cyclohexyl ester(82095-85-0)
EPA Substance Registry System: (1R,3S)-3-(2-Chloro-ethyl)-2,2-dimethyl-cyclopropanecarboxylic acid 2-isopropyl-5-methyl-cyclohexyl ester(82095-85-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 82095-85-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82095-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,9 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82095-85:
(7*8)+(6*2)+(5*0)+(4*9)+(3*5)+(2*8)+(1*5)=140
140 % 10 = 0
So 82095-85-0 is a valid CAS Registry Number.

82095-85-0Upstream product

7712-60-9 5-chloro-2-methyl-pent-2-ene

82095-85-0Downstream Products

82095-85-0Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS OF PERMETHRIC ACID. STEREOCHEMISTRY OF CHIRAL COPPER CARBENOID REACTION.

Aratani, Tadatoshi,Yoneyoshi, Yukio,Nagase, Tsuneyuki

, p. 685 - 688 (1982)

The most effective optical isomer (1R-cis) of permethric acid (2, R=H), a potent intermediate in the production of synthetic pyrethroid, was enantioselectively prepared.

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