Cas 155687-80-2,(1R,2S,3R,6S)-3,6-Dimethyl-1-((S)-toluene-4-sulfinyl)-cyclohex-4-ene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

155687-80-2

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Basic information

Product Name: (1R,2S,3R,6S)-3,6-Dimethyl-1-((S)-toluene-4-sulfinyl)-cyclohex-4-ene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
Synonyms:
CAS NO:155687-80-2
Molecular Formula:
Molecular Weight: 440.56
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,2S,3R,6S)-3,6-Dimethyl-1-((S)-toluene-4-sulfinyl)-cyclohex-4-ene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3R,6S)-3,6-Dimethyl-1-((S)-toluene-4-sulfinyl)-cyclohex-4-ene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(155687-80-2)
EPA Substance Registry System: (1R,2S,3R,6S)-3,6-Dimethyl-1-((S)-toluene-4-sulfinyl)-cyclohex-4-ene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(155687-80-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 155687-80-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155687-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,8 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 155687-80:
(8*1)+(7*5)+(6*5)+(5*6)+(4*8)+(3*7)+(2*8)+(1*0)=172
172 % 10 = 2
So 155687-80-2 is a valid CAS Registry Number.

155687-80-2Upstream product

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155687-80-2Relevant academic research and scientific papers

Benzyl Methyl (S)-2-(p-Tolylsulfinyl)maleate: An Efficient Dienophile for the Enantioselective Synthesis of Cyclohexadienes

Alonso, Ines,Carretero, Juan C.,Ruano, Jose L. Garcia

, p. 3231 - 3232 (2007/10/02)

The new dienophile, benzyl methyl (S)-2-(p-tolylsulfinyl)maleate, readily prepared in two steps from benzyl acetate, reacts with a wide variety of 1,3-dienes, under catalysis by TiCl4, in a very regioselective and stereoselective manner to give optically

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