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3-Oxazolidinecarboxylic acid, 5-oxo-4-(2-oxoethyl)-, phenylmethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111197-45-6

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111197-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111197-45-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111197-45:
(8*1)+(7*1)+(6*1)+(5*1)+(4*9)+(3*7)+(2*4)+(1*5)=96
96 % 10 = 6
So 111197-45-6 is a valid CAS Registry Number.

111197-45-6SDS

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 (S)-4-(Formylmethyl)-5-oxooxazolidin-3-carbonsaeure-benzylester

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:111197-45-6 SDS

111197-45-6Relevant academic research and scientific papers

SYNTHESIS OF BICYCLIC γ-LACTAMS VIA OXAZOLIDINONES

Baldwin, Jack E.,Lee, E.

, p. 6551 - 6554 (1986)

Oxazolidinone aldehyde 10 reacts with L-cysteine methyl ester to produce N-hydroxymethyl bicyclic γ-lactam 11 in a double cyclisation reaction.With D-cysteine methyl ester, an epimeric mixture of N-hydroxymethyl bicyclic γ-lactams 12 is obtained.Bicyclic

Preparation of 'Semialdehyde' Derivatives of Aspartic and Glutamic Acid via the Rosenmund Reduction

Bold, Guido,Steiner, Heinz,Moesch, Luzia,Walliser, Bernhard

, p. 405 - 410 (1990)

Suitable protected aspartic-acid 'β-semialdehyde' and glutamic acid 'γ-aldehyde' derivatives can be obtained, in good yield by Rosenmund reduction of the corresponding acid chlorides.Benzyloxycarbonyl (Z) and (tert-butoxy)carbonyl (Boc) protecting groups

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