Cas 286012-80-4,(S)-2-[(Z)-2-((R)-Toluene-4-sulfinyl)-vinyl]-cyclopent-3-ene-1,1-dicarboxylic acid dimethyl ester

286012-80-4

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Basic information

Product Name: (S)-2-[(Z)-2-((R)-Toluene-4-sulfinyl)-vinyl]-cyclopent-3-ene-1,1-dicarboxylic acid dimethyl ester
Synonyms:
CAS NO:286012-80-4
Molecular Formula:
Molecular Weight: 348.42
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)-2-[(Z)-2-((R)-Toluene-4-sulfinyl)-vinyl]-cyclopent-3-ene-1,1-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(Z)-2-((R)-Toluene-4-sulfinyl)-vinyl]-cyclopent-3-ene-1,1-dicarboxylic acid dimethyl ester(286012-80-4)
EPA Substance Registry System: (S)-2-[(Z)-2-((R)-Toluene-4-sulfinyl)-vinyl]-cyclopent-3-ene-1,1-dicarboxylic acid dimethyl ester(286012-80-4)

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: 286012-80-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 286012-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,6,0,1 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 286012-80:
(8*2)+(7*8)+(6*6)+(5*0)+(4*1)+(3*2)+(2*8)+(1*0)=134
134 % 10 = 4
So 286012-80-4 is a valid CAS Registry Number.

286012-80-4Upstream product

286012-80-4Downstream Products

286012-80-4Relevant academic research and scientific papers

Participation of the chiral sulfinyl functionality in palladium- catalyzed asymmetric vinylcyclopropane-cyclopentene rearrangements

Hiroi, Kunio,Yoshida, Yasuki,Kaneko, Yoko

, p. 3431 - 3434 (2007/10/03)

Stereochemical studies on the palladium-catalyzed asymmetric 1,3- rearrangements of [4-chiral arylsulfinyl-1,3(E or Z)- butadienyl]cyclopropanes to chiral cyclopentenes are described. The plausible mechanism for the rationalization of the stereochemical outcomes is proposed.

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