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1-Azabicyclo[3.2.0]heptane-2-carboxylic acid, 4-(benzoyloxy)-3-chloro-3-(ethylsulfinyl)-6-methyl-7-oxo-, (4-nitrophenyl)methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137439-99-7

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137439-99-7 Usage

Type

Semi-synthetic broad-spectrum cephalosporin antibiotic

Function

Treats a variety of bacterial infections

Application areas

Respiratory and urinary tracts, skin and soft tissue, and bone and joint infections

Mechanism of action

Inhibits bacterial growth

Effectiveness

Active against both gram-positive and gram-negative organisms

Usage

Commonly used in clinical settings to combat bacterial infections

Check Digit Verification of cas no

The CAS Registry Mumber 137439-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,3 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137439-99:
(8*1)+(7*3)+(6*7)+(5*4)+(4*3)+(3*9)+(2*9)+(1*9)=157
157 % 10 = 7
So 137439-99-7 is a valid CAS Registry Number.

137439-99-7SDS

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 p-Nitrobenzyl (4RS,5RS,6RS)-4-benzoyloxy-3-chloro-3-ethylsulphinyl-6-methyl-7-oxo-1-azabicyclo<3.2.0>heptane-2-carboxylate

1.2 Other means of identification

Product number -
Other names (4R,5R,6R)-4-Benzoyloxy-3-chloro-3-ethanesulfinyl-6-methyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

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:137439-99-7 SDS

137439-99-7Relevant academic research and scientific papers

Olivanic Acid Analogues. Part 9. Allylic Oxidative Functionalisation of Substituted Azetidinones: Synthesis of Some 4-Acyloxy-7-oxo-1-azabicyclohept-2-ene-2-carboxylates

Bateson, John H.,Robins, Alison M.,Southgate, Robert

, p. 2399 - 2405 (2007/10/02)

Sharpless oxidation (ButO2H), SeO2) of the protected allyl azetidinone 7 gave the allylic alcohol 8 which was transformed to the 5,6-trans-4α-acetoxyolivanic acid derivative 16.Kharasch-Sosnovsky benzoyloxylation (PhCO3But, CuCl, PhH, heat) of the silylated 7-azabicyclooct-3-enes 17b,c provided inter alia allylic benzoates 18b,c and 21b,c.These were synthetic precursors of the 5,6-cis-olivanic acid analogues 23 and 26, which contain 8- and 4α-benzoyloxy groups, respectively.

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