Cas 811467-31-9,Benzenepropanoic acid, alpha,ba-dihydroxy-2-methyl-, ethyl ester, (alphaR,baR)-rel- (9CI)

811467-31-9

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Basic information

Product Name: Benzenepropanoic acid, alpha,ba-dihydroxy-2-methyl-, ethyl ester, (alphaR,baR)-rel- (9CI)
Synonyms: Benzenepropanoicacid,alpha,bta-dihydroxy-2-methyl-,ethylester,(alphaR,btaR)-rel-(9CI);Benzenepropanoic acid, alpha,ba-dihydroxy-2-methyl-, ethyl ester, (alphaR,baR)-rel- (9CI)
CAS NO:811467-31-9
Molecular Formula: C12H16O4
Molecular Weight: 224.25304
EINECS: N/A
Product Categories: METHYL
Mol File: 811467-31-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzenepropanoic acid, alpha,ba-dihydroxy-2-methyl-, ethyl ester, (alphaR,baR)-rel- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Benzenepropanoic acid, alpha,ba-dihydroxy-2-methyl-, ethyl ester, (alphaR,baR)-rel- (9CI)(811467-31-9)
EPA Substance Registry System: Benzenepropanoic acid, alpha,ba-dihydroxy-2-methyl-, ethyl ester, (alphaR,baR)-rel- (9CI)(811467-31-9)

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: 811467-31-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 811467-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,4,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 811467-31:
(8*8)+(7*1)+(6*1)+(5*4)+(4*6)+(3*7)+(2*3)+(1*1)=149
149 % 10 = 9
So 811467-31-9 is a valid CAS Registry Number.

811467-31-9Upstream product

811467-31-9Downstream Products

811467-31-9Relevant academic research and scientific papers

Stereoselective reduction of β-hydroxy α-ketoesters: A concise synthesis of anti-α,β-dihydroxy esters

Liao, Mingyi,Yao, Wengang,Wang, Jianbo

, p. 2633 - 2636 (2007/10/03)

A new synthetic route to anti-α,β-dihydroxy esters has been developed. The new method consists of three steps starting from an aldehyde: the nucleophilic condensation with ethyl diazoacetate, oxidation with dimethyldioxirane, and stereoselective reduction with NaBH4.

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