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60907-88-2

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60907-88-2 Usage

General Description

1-(2,3-Dimethylphenyl)ethyl chloride is a chemical compound also known as alpha-(2,3-dimethylphenyl)ethyl chloride. It can be categorized under the class of organic compounds known as dimethylbenzenes. They possess an aromatic benzene ring with two methyl groups attached. It is a solid, crystalline substance that is usually white or off-white in color. This chemical has a wide variety of potential uses in the realms of organic synthesis and chemical engineering, largely due to its ability to participate in various types of chemical reactions. Ensuring appropriate safety measures is important while handling it as it can be harmful if inhaled, if it comes in contact with skin, or if swallowed.

Check Digit Verification of cas no

The CAS Registry Mumber 60907-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,0 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60907-88:
(7*6)+(6*0)+(5*9)+(4*0)+(3*7)+(2*8)+(1*8)=132
132 % 10 = 2
So 60907-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13Cl/c1-7-5-4-6-10(8(7)2)9(3)11/h4-6,9H,1-3H3

60907-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-chloroethyl)-2,3-dimethylbenzene

1.2 Other means of identification

Product number -
Other names AC-5605

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:60907-88-2 SDS

60907-88-2Upstream product

60907-88-2Relevant articles and documents

Process for the preparation of substituted vinylbenzyl chloride

-

, (2008/06/13)

An improved continous single step vapor phase process for the preparation of substituted vinylbenzyl chloride from substituted ethyltoluene is disclosed. In this process a substituted ethyltoluene is reacted with a halogen gas in the vapor phase, at elevated temperatures via a continuous feed process. Furthermore, this process achieves halogenation followed by dehydrohalogenation in a single pass through the reactor. There is also obtained a very high total selectivity to vinylbenzyl chloride and its precursors via this continuous process.

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