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136171-94-3

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136171-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136171-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 136171-94:
(8*1)+(7*3)+(6*6)+(5*1)+(4*7)+(3*1)+(2*9)+(1*4)=123
123 % 10 = 3
So 136171-94-3 is a valid CAS Registry Number.

136171-94-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2S,3R)-3-(hydroxymethyl)oxirane-2-carboxylate

1.2 Other means of identification

Product number -
Other names Oxiranecarboxylic acid,3-(hydroxymethyl)-,ethyl ester,(2S-trans)-(9CI)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:136171-94-3 SDS

136171-94-3Relevant articles and documents

Organocatalytic asymmetric epoxidation reactions in water-alcohol solutions

Zhuang, Wei,Marigo, Mauro,Jorgensen, Karl Anker

, p. 3883 - 3885 (2007/10/03)

The diastereo- and enantioselective organocatalytic epoxidation of α,β-unsaturated aldehydes in aqueous solutions is presented. By the screening of the reaction conditions for the epoxidation of cinnamic aldehyde applying hydrogen peroxide as the oxidant and 2-[bis-(3,5-bis-trifluoromethyl- phenyl)-trimethylsilanyloxy-methyl]-pyrrolidine as the catalyst, a highly stereoselective reaction has been developed. The scope of the diastereo- and enantioselective organocatalytic epoxidation in aqueous solutions is documented by the asymmetric epoxidation of α,β-unsaturated aldehydes with enantioselectivities up to 96% ee. The Royal Society of Chemistry 2005.

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