Cas 134940-39-9,(1S,2S,3R,4R)-Bicyclo[2.2.1]heptane-2,3-dicarboxylic acid mono-((R)-benzyloxycarbonyl-phenyl-methyl) ester

134940-39-9

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Basic information

Product Name: (1S,2S,3R,4R)-Bicyclo[2.2.1]heptane-2,3-dicarboxylic acid mono-((R)-benzyloxycarbonyl-phenyl-methyl) ester
Synonyms:
CAS NO:134940-39-9
Molecular Formula:
Molecular Weight: 408.451
EINECS: N/A
Product Categories: N/A
Mol File: 134940-39-9.mol
Article Data: 1

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: (1S,2S,3R,4R)-Bicyclo[2.2.1]heptane-2,3-dicarboxylic acid mono-((R)-benzyloxycarbonyl-phenyl-methyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3R,4R)-Bicyclo[2.2.1]heptane-2,3-dicarboxylic acid mono-((R)-benzyloxycarbonyl-phenyl-methyl) ester(134940-39-9)
EPA Substance Registry System: (1S,2S,3R,4R)-Bicyclo[2.2.1]heptane-2,3-dicarboxylic acid mono-((R)-benzyloxycarbonyl-phenyl-methyl) ester(134940-39-9)

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: 134940-39-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134940-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,4 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134940-39:
(8*1)+(7*3)+(6*4)+(5*9)+(4*4)+(3*0)+(2*3)+(1*9)=129
129 % 10 = 9
So 134940-39-9 is a valid CAS Registry Number.

134940-39-9Upstream product

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134940-39-9Relevant articles and documents

Highly Effective and Practical Enantioselective Synthesis of Half-Esters of Bicycloheptanedicarboxylic Acid

Ohtani, Mitsuaki,Matsuura, Takaharu,Watanabe, Fumihiko,Narisada, Masayuki

, p. 4120 - 4123 (2007/10/02)

An effective and practical enantioselective synthesis of half-esters of bicycloheptane-2,3-dicarboxylic acid was developed by enantioselective fission of ?-symmetrical cyclic anhydrides with chiral mandelic acid derivatives, followed by deprotectio

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