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2-Azetidinone, 4-(4-chlorophenyl)-1,3-diphenyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62500-55-4

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62500-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62500-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,0 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62500-55:
(7*6)+(6*2)+(5*5)+(4*0)+(3*0)+(2*5)+(1*5)=94
94 % 10 = 4
So 62500-55-4 is a valid CAS Registry Number.

62500-55-4SDS

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 (3S,4R)-4-(4-chlorophenyl)-1,3-diphenylazetidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Azetidinone,4-(4-chlorophenyl)-1,3-diphenyl-,trans

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:62500-55-4 SDS

62500-55-4Downstream Products

62500-55-4Relevant academic research and scientific papers

Synthesis and antimicrobial activity of 1,3,4-triaryl-2-azetidinones

Diurno,Mazzoni,Piscopo,Bolognese

, p. 239 - 247 (2007/10/02)

A set of substituted 1,3,4-triaryl-2-azetidinones were synthesized and characterized. Their antimicrobial activity, against Gram+ and Gram- bacteria and Fungi, was tested. The compounds 23 and 30 showed remarkable activity against Pseudomonas aeruginosa.

On the azetidin-2-one ring formation. A 1H NMR investigation

Bolognese, Adele,Diurno, M. Vittoria,Mazzoni, Orazio,Giordano, Federico

, p. 7417 - 7428 (2007/10/02)

Azetidin-2-ones were prepared by addition of phenylacetic acid chloride to substituted benzal-anilines in DMF. The effect of temperature and substituents at the benzal-anilines on the reaction mechanism was investigated carrying out the reaction in DMF d7 in an NMR probe of a Bruker 400-MHz spectrometer at 25 and 60°C. Proton signals, arising from two kinds of intermediates a 2-phenyl-N-(α-chlorobenzyl)-acetanilide (6) and a nitrogen-charged adduct (7) suggest that two competitive mechanisms play a role in the formation of trans and cis azetidin-2-ones.

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