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113337-40-9

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113337-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113337-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113337-40:
(8*1)+(7*1)+(6*3)+(5*3)+(4*3)+(3*7)+(2*4)+(1*0)=89
89 % 10 = 9
So 113337-40-9 is a valid CAS Registry Number.

113337-40-9SDS

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 2,2-dichloro-1-(2,6-dimethylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2,2-DICHLORO-1-(2,6-DIMETHYLPHENYL)-ETHANONE

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:113337-40-9 SDS

113337-40-9Upstream product

113337-40-9Downstream Products

113337-40-9Relevant articles and documents

INVESTIGATIONS ON REACTIONS OF CHLORINE DIOXIDE AND SODIUM CHLORITE WITH ORGANIC COMPOUNDS. PART XXXV. REACTIONS OF CHLORINE DIOXIDE WITH RING-SUBSTITUTED STYRENES

Kwiecien, Halina,Jalowiczor, Jozef

, p. 811 - 824 (2007/10/02)

Reactions of chlorine dioxide with ring substituted styrenes (1a-n) in carbon tetrachloride at 52-54 deg C were studied.The reaction products were isolated and characterised.It has been found that methyl-, chloro-, nitrostyrenes and 4-methoxystyrene are attacked by chlorine dioxide exclusively on the vinyl group, to yield the corresponding α-chloroacetophenones (2), diastereoisomers of β-chlorostyrene (6,7), oxidation products (8,9) and some polymers.Oxidation of its phenolic hydroxyl groups and vinyl polymerization took place in hydroxystyrenes.

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