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CAS

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82933-25-3

Benzeneacetamide, N-(1-hydroxy-2-oxo-3-azetidinyl)-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82933-25-3

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82933-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82933-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82933-25:
(7*8)+(6*2)+(5*9)+(4*3)+(3*3)+(2*2)+(1*5)=143
143 % 10 = 3
So 82933-25-3 is a valid CAS Registry Number.

82933-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-(1-Hydroxy-2-oxo-3-azetidinyl)-2-phenylacetamide

1.2 Other means of identification

Product number -
Other names (S)-1-Hydroxy-3-[(phenylacetyl)amino]-2-azetidinone

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:82933-25-3 SDS

82933-25-3Relevant articles and documents

Practical synthetic approaches to intermediates for the preparations of the novel O-sulfonated-N-hydroxy-2-azetidinone antibiotics

Miller,Biswas,Krook

, p. 2571 - 2575 (1983)

A practical synthesis of intermediates useful for the preparation of a variety of monocyclic β-lactam antibiotics is described. Hydroxaminolysis of N-protected serine esters provided the hydroxamic acids 10. Acylation followed by cyclization yielded the β

O-sulfated β-lactam hydroxamic acids and intermediates

-

, (2008/06/13)

Antibacterial activity is exhibited by β-lactams having a sulfate substituent in the 1-position and an acylamino substituent in the 3-position.

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