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2-Azetidinecarboxylic acid, 4-oxo-1-(phenylmethyl)-, methyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116156-31-1

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116156-31-1 Usage

Molar mass

219.24 g/mol

Specific rotation

(S)-configuration

Common use

Building block in pharmaceutical synthesis

Chirality

Potential applications in medicinal chemistry and drug design

Biological and pharmacological properties

Studied for potential effects
Target for research and development in pharmaceutical sciences

Check Digit Verification of cas no

The CAS Registry Mumber 116156-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,5 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116156-31:
(8*1)+(7*1)+(6*6)+(5*1)+(4*5)+(3*6)+(2*3)+(1*1)=101
101 % 10 = 1
So 116156-31-1 is a valid CAS Registry Number.

116156-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-1-benzyl-4-oxoazetidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Azetidinecarboxylic acid,4-oxo-1-(phenylmethyl)-,methyl ester,(S)

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:116156-31-1 SDS

116156-31-1Downstream Products

116156-31-1Relevant academic research and scientific papers

HIGHLY EFFICIENT OXAZOLONE-DERIVED REAGENTS FOR BETA-LACTAM FORMATION FROM BETA-AMINO ACIDS

Kunieda, Takehisa,Nagamatsu, Tomohisa,Higuchi, Tsunehiko,Hirobe, Masaaki

, p. 2203 - 2206 (1988)

Based on a unique leaving ability of 2-oxazolone moiety, highly efficient reagents have been developed for the formation of β-lactam compounds from β-amino acids including a facile preparation of penam, a basic skeleton of penicillins.

A NOVEL METHOD FOR THE SYNTHESIS OF β-LACTAMS BY MEANS OF PHASE TRANSFER SYSTEM

Watanabe, Yutaka,Mukaiyama, Teruaki

, p. 443 - 444 (1981)

The reaction of β-amino acids with methanesulfonyl chloride in a chloroform-water bilayer system in the presence of 15 molpercent of tetrabutylammonium hydrogen sulfate gives the corresponding β-lactams in good yields.

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