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106260-02-0

2-Propanone, 1-chloro-3-(2-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106260-02-0

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106260-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106260-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,6 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106260-02:
(8*1)+(7*0)+(6*6)+(5*2)+(4*6)+(3*0)+(2*0)+(1*2)=80
80 % 10 = 0
So 106260-02-0 is a valid CAS Registry Number.

106260-02-0SDS

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 Chloroacetonylpyridine

1.2 Other means of identification

Product number -
Other names 1-chloro-3-(pyridine-2-yl)propan-2-one

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:106260-02-0 SDS

106260-02-0Downstream Products

106260-02-0Relevant articles and documents

TAUTOMERISM OF AZINE DERIVATIVES. 11. 14N-NMR AND 17O-NMR INVESTIGATION OF INTRACHELATE TAUTOMERISM OF ACYLMETHYLPYRIDINES

Lapachev, V. V.,Stekhova, S. A.,Mainagashev, I. Ya.,Fedotov, M. A.,Khall, V. E.,Mamaev, V. P.

, p. 633 - 639 (2007/10/02)

Intrachelate -sigmatropic tautomerism in a series of acylmethylpyridines has been studied by 14N- and 17O-NMR specroscopy.Principles of tautomer modelling or simulation have been proposed and examined, nitrogen ond oxygen chemical shift spectra have been determined, and the accuracy of this method for the determination of tautomer composition has been evaluated.The presence of acceptor (electron withdrawing) substituents in the acylmethyl side-chain fragment has been found to stabilize the NH-tautomer.

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