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5326-06-7

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5326-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5326-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5326-06:
(6*5)+(5*3)+(4*2)+(3*6)+(2*0)+(1*6)=77
77 % 10 = 7
So 5326-06-7 is a valid CAS Registry Number.

5326-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [amino(ethoxy)phosphoryl]benzene

1.2 Other means of identification

Product number -
Other names O-Ethyl-benzolphosphonsaeureesteramid

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:5326-06-7 SDS

5326-06-7Downstream Products

5326-06-7Relevant articles and documents

Phosphonamidates are the first phosphorus-based zinc binding motif to show inhibition of β-class carbonic anhydrases from bacteria, fungi, and protozoa

Alissa, Siham A.,Alghulikah, Hanan A.,Alothman, Zeid A.,Osman, Sameh M.,Del Prete, Sonia,Capasso, Clemente,Nocentini, Alessio,Supuran, Claudiu T.

, p. 59 - 64 (2019/11/11)

A primary strategy to combat antimicrobial resistance is the identification of novel therapeutic targets and anti-infectives with alternative mechanisms of action. The inhibition of the metalloenzymes carbonic anhydrases (CAs, EC 4.2.1.1) from pathogens (

PHOSPHORUS ANALOGUES OF AMINO ACIDS AND PEPTIDES XII. REACTION OF SODIUM DIETHYL PHOSPHITE WITH AROMATIC ALDAZINES AND HYDRAZONES

Topolski, M.,Rachon, J.

, p. 97 - 110 (2007/10/02)

The mechanism of the reaction of sodium diethyl phosphite with aromatic aldazines has been investigated.The initially formed monoaddition product (4) reacts with the excess of phosphorus reagent prior to the conceivable addition of diethyl phosphite to the C=N double bond.Cleavage of the N-N single bond is initiated by Single Electron Transfer from phosphite anion to the conjugated N=CH-Ph bond system.The scope of the reaction can be extended to other aromatic hydrazones.There is strong evidence to support the operation of a non-chain SET mechanism.

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