Cas 162780-55-4,(S)-5,6,7,8,9,9a-Hexahydro-3H-benzocycloheptene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

162780-55-4

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Basic information

Product Name: (S)-5,6,7,8,9,9a-Hexahydro-3H-benzocycloheptene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
Synonyms: (S)-5,6,7,8,9,9a-Hexahydro-3H-benzocycloheptene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
CAS NO:162780-55-4
Molecular Formula:
Molecular Weight: 340.419
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)-5,6,7,8,9,9a-Hexahydro-3H-benzocycloheptene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-5,6,7,8,9,9a-Hexahydro-3H-benzocycloheptene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(162780-55-4)
EPA Substance Registry System: (S)-5,6,7,8,9,9a-Hexahydro-3H-benzocycloheptene-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(162780-55-4)

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: 162780-55-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 162780-55-4 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 162780-55:
(8*1)+(7*6)+(6*2)+(5*7)+(4*8)+(3*0)+(2*5)+(1*5)=144
144 % 10 = 4
So 162780-55-4 is a valid CAS Registry Number.

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162780-55-4Relevant 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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