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2-Azetidinecarboxylic acid, 3-ethenyl-1-(4-methoxyphenyl)-4-oxo-, ethyl ester, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119873-85-7

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119873-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119873-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,7 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119873-85:
(8*1)+(7*1)+(6*9)+(5*8)+(4*7)+(3*3)+(2*8)+(1*5)=167
167 % 10 = 7
So 119873-85-7 is a valid CAS Registry Number.

119873-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1-p-Methoxyphenyl-3-vinyl-4-ethoxycarbonylazetidinone

1.2 Other means of identification

Product number -
Other names cis-1-p-anisyl-3-vinyl-4-carbethoxy-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:119873-85-7 SDS

119873-85-7Relevant academic research and scientific papers

Monocyclic β-lactam inhibitors of human leukocyte elastase

Firestone,Barker,Pisano,Ashe,Dahlgren

, p. 2255 - 2262 (2007/10/02)

Two types of monocyclic azetidinones have been synthesized that were designed to inactivate human leukocyte elastase (HLE) in three steps: first, acylation of active-site serine; second, creation of a powerful new electrophilic center; third, covalent cap

β-Lactams via α,β-Unsaturated Acid Chlorides: Intermediates for Carbapenem Antibiotics

Manhas, M. S.,Ghosh, Malay,Bose, Ajay K.

, p. 575 - 580 (2007/10/02)

Stereocontrolled synthesis of α-vinyl β-lactams and their transformation to convenient intermediates for PS-5, PS-6, asparenomycin, and thienamycin are described.

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