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853737-95-8

853737-95-8

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853737-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853737-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,7,3 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 853737-95:
(8*8)+(7*5)+(6*3)+(5*7)+(4*3)+(3*7)+(2*9)+(1*5)=208
208 % 10 = 8
So 853737-95-8 is a valid CAS Registry Number.

853737-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-2-nitrobenzenesulfonyl-((R)-2-hydroxybutyl)carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names -

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:853737-95-8 SDS

853737-95-8Relevant articles and documents

Direct catalytic synthesis of enantiopure 5-substituted oxazolidinones from racemic terminal epoxides

Bartoli, Giuseppe,Bosco, Marcella,Carlone, Armando,Locatelli, Manuela,Melchiorre, Paolo,Sambri, Letizia

, p. 1983 - 1985 (2007/10/03)

(Chemical Equation Presented) A venerable scaffold for asymmetric synthesis and drug development, chiral 5-substituted oxazolidinones are obtained in almost enantiomerically pure form (up to 99.9% ee) starting from racemic terminal epoxides. The salient features of this process include the very simple and convenient experimental protocol and the employment of a readily accessible catalyst and inexpensive, easily handled starting materials. An enantioconvergent approach for the total conversion of racemic epoxide into a single stereoisomeric oxazolidinone is also described.

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