Cas 155485-57-7,2-Chloro-4-cyclohexyl-2,3,3-trifluoro-cyclobutanecarboxylic acid methyl ester

155485-57-7

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Basic information

Product Name: 2-Chloro-4-cyclohexyl-2,3,3-trifluoro-cyclobutanecarboxylic acid methyl ester
Synonyms:
CAS NO:155485-57-7
Molecular Formula:
Molecular Weight: 284.706
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: 2-Chloro-4-cyclohexyl-2,3,3-trifluoro-cyclobutanecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Chloro-4-cyclohexyl-2,3,3-trifluoro-cyclobutanecarboxylic acid methyl ester(155485-57-7)
EPA Substance Registry System: 2-Chloro-4-cyclohexyl-2,3,3-trifluoro-cyclobutanecarboxylic acid methyl ester(155485-57-7)

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: 155485-57-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155485-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,4,8 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 155485-57:
(8*1)+(7*5)+(6*5)+(5*4)+(4*8)+(3*5)+(2*5)+(1*7)=157
157 % 10 = 7
So 155485-57-7 is a valid CAS Registry Number.

155485-57-7Upstream product

139008-27-8 methyl 1-phenylthio-2-chloro-2,3,3-trifluorocyclobutane carboxylate

155485-57-7Downstream Products

155485-57-7Relevant academic research and scientific papers

Activation of acrylate-moiety by strain and fluoroalkyl substitution in 4-chloro-3,3,4-trifluoromethoxycarbonyl cyclobutene

Plancquaert, Marie-Aimee,Francois, Philippe,Merenyi, Robert,Viehe, Heinz G.

, p. 7265 - 7268 (1991)

A two step preparation is reported for the title cyclobutene derivative 3 starting from 2-phenylthioacrylate 1 and chlorotrifluoroethylene followed by oxidative elimination. Strain and polarity facilitate reactions with nucleophiles, radicals, dienes and diazoalkanes.

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