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57072-35-2

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57072-35-2 Usage

General Description

5'-NUCLEOTIDE PHOSPHODIESTERASE SUBSTRATE is a chemical compound that serves as a substrate for the enzyme 5'-nucleotide phosphodiesterase. This enzyme catalyzes the hydrolysis of the phosphodiester bond within a 5'-nucleotide, resulting in the release of a phosphate group and the formation of a nucleotide with a free 5'-hydroxyl group. The substrate is typically used in enzymatic assays to study the activity of 5'-nucleotide phosphodiesterase and to screen for inhibitors or activators of the enzyme. It is also used in biochemical research to investigate the mechanisms and kinetics of nucleotide hydrolysis.

Check Digit Verification of cas no

The CAS Registry Mumber 57072-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,7 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57072-35:
(7*5)+(6*7)+(5*0)+(4*7)+(3*2)+(2*3)+(1*5)=122
122 % 10 = 2
So 57072-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H10NO5P/c14-13(15)10-6-8-11(9-7-10)18-19(16,17)12-4-2-1-3-5-12/h1-9H,(H,16,17)/p-1

57072-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenoxy)-phenylphosphinic acid

1.2 Other means of identification

Product number -
Other names phenylphosphonic acid bis-(4-nitrophenyl)-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:57072-35-2 SDS

57072-35-2Relevant articles and documents

Hydrolysis of 4-Nitrophenyl Phenyl(trichloromethyl)phosphinate: Predominance of a P-C vs P-O Bond Cleavage Reaction

Hammond, Philip S.,Kirchner, Michael B.,Lieske, Claire N.

, p. 6049 - 6051 (2007/10/02)

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PHOSPHONATE MONOESTERS AND METHOD OF PREPARATION

-

, (2008/06/13)

Synthesis of phosphonate monoesters, as well as the use of such monoesters as substrates for enzymes which normally hydrolyze phosphodiester linkages, and a method for distinguishing between Type I and Type II phosphodiesterase enzymes using such monoeste

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