Cas 168103-72-8,(1R,4R,5R)-5-(Hydroxy-diphenyl-methyl)-3,3-diphenyl-2,6,7-trioxa-bicyclo[2.2.1]heptane-1-carboxylic acid methoxy-methyl-amide

168103-72-8

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Basic information

Product Name: (1R,4R,5R)-5-(Hydroxy-diphenyl-methyl)-3,3-diphenyl-2,6,7-trioxa-bicyclo[2.2.1]heptane-1-carboxylic acid methoxy-methyl-amide
Synonyms:
CAS NO:168103-72-8
Molecular Formula:
Molecular Weight: 523.585
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,4R,5R)-5-(Hydroxy-diphenyl-methyl)-3,3-diphenyl-2,6,7-trioxa-bicyclo[2.2.1]heptane-1-carboxylic acid methoxy-methyl-amide(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4R,5R)-5-(Hydroxy-diphenyl-methyl)-3,3-diphenyl-2,6,7-trioxa-bicyclo[2.2.1]heptane-1-carboxylic acid methoxy-methyl-amide(168103-72-8)
EPA Substance Registry System: (1R,4R,5R)-5-(Hydroxy-diphenyl-methyl)-3,3-diphenyl-2,6,7-trioxa-bicyclo[2.2.1]heptane-1-carboxylic acid methoxy-methyl-amide(168103-72-8)

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: 168103-72-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 168103-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,1,0 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 168103-72:
(8*1)+(7*6)+(6*8)+(5*1)+(4*0)+(3*3)+(2*7)+(1*2)=128
128 % 10 = 8
So 168103-72-8 is a valid CAS Registry Number.

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168103-72-8Relevant academic research and scientific papers

A Novel Bicyclic Orthoester as a Chiral Auxiliary: Application to the Synthesis of α-Hydroxy Acids

Dube, D.,Deschenes, D.,Tweddell, J.,Gagnon, H.,Carlini, R.

, p. 1827 - 1830 (1995)

Chiral α-keto orthoesters derived from tartanic acid can be reduced diastereoselectively.Hydrolysis affords optically actice α-hydroxy acids and the recovered auxiliary.

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