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64896-38-4

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64896-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64896-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,9 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64896-38:
(7*6)+(6*4)+(5*8)+(4*9)+(3*6)+(2*3)+(1*8)=174
174 % 10 = 4
So 64896-38-4 is a valid CAS Registry Number.

64896-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-2-(((3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl)methylene)amino)propanoic acid

1.2 Other means of identification

Product number -
Other names -

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:64896-38-4 SDS

64896-38-4Relevant articles and documents

Reaction Kinetics and Equilibria of β-Elimination of Some Schiff Base Complexes

Tatsumoto, Kuniyasu,Martell, Arthur E.,Motekaitis, Ramunas J.

, p. 6197 - 6203 (1981)

The kinetics of β-elimination of O-phosphoserine, β-chloroalanine, S-ethylcysteine, and β-chloro-α-aminobutyric acid was investigated by NMR in deuterium oxide media at 31.5 +/- 0.5 deg C in the presence of pyridoxal and in the presence and the absence of Ga(III), Al(III), and Zn(II) ions.The reaction rate constants and relevant equilibrium constants are reported for these systems.The specific rate constants for the individual molecular species in solution were determined from the observed reaction rate cobstants and equilibrium constants applicable to these systems.Catalysis by pyridoxal in the absence of metal ions showed an increase in rate as pD was increased, with a rate maximum in the region of pD 8-9, and moderate decrease at higher pH.The first-order rate constants varied with the amino acid moiety in the order β-chloroalanine > O-phosphoserine > β-chloro-α-aminobutyric acid > S-ethylcysteine.The rate constants reported for pyridoxal catalysis in the presence of metal ions show rate enhancements in the order of ten times the values of metal-free systems.Possible mechanisms of these reactions are discussed.

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