Cas 162780-54-3,(S)-3,5,6,7,8,8a-Hexahydro-naphthalene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

162780-54-3

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Basic information

Product Name: (S)-3,5,6,7,8,8a-Hexahydro-naphthalene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
Synonyms: (S)-3,5,6,7,8,8a-Hexahydro-naphthalene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
CAS NO:162780-54-3
Molecular Formula:
Molecular Weight: 326.392
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)-3,5,6,7,8,8a-Hexahydro-naphthalene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3,5,6,7,8,8a-Hexahydro-naphthalene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(162780-54-3)
EPA Substance Registry System: (S)-3,5,6,7,8,8a-Hexahydro-naphthalene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(162780-54-3)

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: 162780-54-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 162780-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,7,8 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 162780-54:
(8*1)+(7*6)+(6*2)+(5*7)+(4*8)+(3*0)+(2*5)+(1*4)=143
143 % 10 = 3
So 162780-54-3 is a valid CAS Registry Number.

162780-54-3Upstream product

162780-54-3Downstream Products

162780-54-3Relevant academic research and scientific papers

A Highly Enantioselective Approach to Functionalized Bicyclic Compounds

Carretero, Juan C.,Ruano, Jose L. Garcia,Cabrejas, Luisa M. Martin

, p. 5895 - 5898 (2007/10/02)

The Diels-Alder reaction of benzyl, methyl (S)-2-(p-tolylsulfinyl) maleate with several 1-vinylcycloalkenes, catalyzed by TiCl4, occured with complete regio and stereoselectivity.The regioselectivity of the sulfinyl elimination from the adducts, as well a

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