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Diethyl (N-metachlorobenzylideneaminomethyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1132709-92-2

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1132709-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1132709-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,2,7,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1132709-92:
(9*1)+(8*1)+(7*3)+(6*2)+(5*7)+(4*0)+(3*9)+(2*9)+(1*2)=132
132 % 10 = 2
So 1132709-92-2 is a valid CAS Registry Number.

1132709-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl N-(3-chlorobenzylidene)aminomethylphosphonate

1.2 Other means of identification

Product number -
Other names diethyl {[(3-chlorobenzylidene)amino]methyl}phosphonate

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:1132709-92-2 SDS

1132709-92-2Relevant academic research and scientific papers

Aminophosphonic acids and aminobis(phosphonic acids) as potential inhibitors of penicillin-binding proteins

Beck, Josephine,Gharbi, Sonia,Herteg-Fernea, Adriana,Vercheval, Lionel,Bebrone, Carine,Lassaux, Patricia,Zervosen, Astrid,Marchand-Brynaert, Jacqueline

experimental part, p. 85 - 97 (2009/06/18)

Aminophosphonic acids and aminobis(phosphonic acids) have been prepared by the alkylation of Schiff bases with methyl bromoacetate or ethyl acrylate. Other pathways, like the modified Pudovik reaction and Kabachnik-Fields reaction, have been considered for the synthesis of the α-phosphonic bioisoster of aminocitrate. Partial or complete deprotection of the phosphonate ester have been realised by either acidic hydrolysis or by treatment with trimethylsilyl bromide. Evaluation against penicillin-binding proteins has shown that our compounds are modest inhibitors of class A β-lactamases, but have an interesting activity against R39 (D,D-peptidase/carboxypeptidase). Wiley-VCH Verlag GmbH & Co. KGaA, 2009.

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