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4395-79-3

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4395-79-3 Usage

General Description

2-Chloro-1-methyl-4-(1-methylethyl)benzene, also known as p-cumyl chloride, is a chemical compound with the molecular formula C10H13Cl. It is a chlorinated derivative of cumene, and it is commonly used as an intermediate in the production of pharmaceuticals and agrochemicals. p-Cumyl chloride is a colorless liquid with a strong, sweet odor, and it is primarily used as a building block for the synthesis of a variety of organic compounds. It is also used in the production of polycarbonates and other high-performance polymers. However,

Check Digit Verification of cas no

The CAS Registry Mumber 4395-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4395-79:
(6*4)+(5*3)+(4*9)+(3*5)+(2*7)+(1*9)=113
113 % 10 = 3
So 4395-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13Cl/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7H,1-3H3

4395-79-3SDS

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-Chloro-4-isopropyltoluene

1.2 Other means of identification

Product number -
Other names 2-monochloro-p-cymene

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:4395-79-3 SDS

4395-79-3Relevant articles and documents

Efficient synthesis of vinyl chlorides and/or gem-dichlorides from ketones by treatment with tungsten hexachloride

Jung, Michael E.,Wasserman, Jacob I.

, p. 7273 - 7275 (2007/10/03)

Treatment of cyclic ketones, e.g. 4, with tungsten hexachloride (WCl 6) provided good yields of vinyl chlorides, e.g. 5, and/or gem-dichlorides. A trans-diequatorial dichloride 9 was prepared by treatment of the corresponding epoxide 8 with WCl

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