Cas 213531-63-6,(S)-3-Cyclohexylidene-4-(1-methoxy-1-methyl-ethyl)-cyclopentane-1,1-dicarboxylic acid dimethyl ester

213531-63-6

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Basic information

Product Name: (S)-3-Cyclohexylidene-4-(1-methoxy-1-methyl-ethyl)-cyclopentane-1,1-dicarboxylic acid dimethyl ester
Synonyms: (S)-3-Cyclohexylidene-4-(1-methoxy-1-methyl-ethyl)-cyclopentane-1,1-dicarboxylic acid dimethyl ester
CAS NO:213531-63-6
Molecular Formula:
Molecular Weight: 338.444
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: (S)-3-Cyclohexylidene-4-(1-methoxy-1-methyl-ethyl)-cyclopentane-1,1-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-Cyclohexylidene-4-(1-methoxy-1-methyl-ethyl)-cyclopentane-1,1-dicarboxylic acid dimethyl ester(213531-63-6)
EPA Substance Registry System: (S)-3-Cyclohexylidene-4-(1-methoxy-1-methyl-ethyl)-cyclopentane-1,1-dicarboxylic acid dimethyl ester(213531-63-6)

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: 213531-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213531-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,5,3 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 213531-63:
(8*2)+(7*1)+(6*3)+(5*5)+(4*3)+(3*1)+(2*6)+(1*3)=96
96 % 10 = 6
So 213531-63-6 is a valid CAS Registry Number.

213531-63-6Upstream product

213531-63-6Downstream Products

213531-63-6Relevant academic research and scientific papers

Asymmetric intramolecular radical vinylation using enantiopure sulfoxides as temporary chiral auxiliaries

Delouvrié, Bénédicte,Fensterbank, Louis,Lac?te, Emmanuel,Malacria, Max

, p. 11395 - 11401 (2007/10/03)

A very diastereoselective addition-elimination sequence affords cyclopentane derivatives in high enantiomeric purities. The enantiopure sulfoxide unit serves as a very efficient temporary chiral auxiliary in this tandem reaction. Interestingly, the presen

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