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Benzene, 1-(1-chloro-1-methylethyl)-4-methyl-, also known as 1-(1-chloro-1-methylethyl)-4-methylbenzene or 1-(1-chloro-1-methylethyl)-4-methylbenzene, is an organic compound with the molecular formula C10H13Cl. It is a derivative of benzene, featuring a chloromethylethyl group at the 1-position and a methyl group at the 4-position. Benzene, 1-(1-chloro-1-methylethyl)-4-methyl- is characterized by its aromatic structure and the presence of a chlorine atom, which can participate in various chemical reactions, such as nucleophilic substitutions. It is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds due to its reactive nature and the ability to form stable intermediates in chemical transformations.

7243-79-0

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7243-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7243-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7243-79:
(6*7)+(5*2)+(4*4)+(3*3)+(2*7)+(1*9)=100
100 % 10 = 0
So 7243-79-0 is a valid CAS Registry Number.

7243-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloropropan-2-yl)-4-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-methyl-4-(1-chloro-1-methylethyl)

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:7243-79-0 SDS

7243-79-0Relevant academic research and scientific papers

Kinetics of elimination reactions of cumyl chloride and its substituted derivatives in acetonitrile

Balachandran,Santhosh Kumar

, p. 1731 - 1734 (2007/10/03)

A cent per cent unimolecular elimination reaction of tertiary aralkyl halides in acetonitrile is being reported for the first time. The reversibility in the rate determining step can be prevented by the addition of a weak base like pyridine in cumyl chloride and its α- and p-substituted derivatives. A plot of logarithmic rate constants of α-substituted cumyl chloride against Charton's steric parameter 'v' gives a linear relationship.

Interpretation of retention indices in gas chromatography for establishing structures of isomeric products of alkylarenes radical chlorination

Zenkevich

, p. 270 - 280 (2007/10/03)

By an example of previously uncharacterized products obtained by alkylarenes radical chlorination was demonstrated that combination of various interpretation methods applied to the retention indices (RI) in the gas chromatography on the standard nonpolar phases (comparison of RI of products and initial compounds, characteristics of succession of the chromatographic elution of the structural isomers with the use of estimation of molecular dynamic parameters, application of the additive schemes to RI calculation, and using of structural analogy CH3?Cl for testing the results obtained) permitted unambiguous identification of the structure even without data of mass spectrometry.

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