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Methanone, (2,4-dichlorophenyl)(4-methylphenyl)-, also known as bis(2,4-dichlorophenyl)(4-methylphenyl)methanone, is an organic compound with the chemical formula C15H10Cl2O. It is a derivative of acetophenone, featuring a carbonyl group (C=O) bonded to two aryl groups. The molecule consists of a central carbon atom double-bonded to an oxygen atom, with two different substituted phenyl rings attached to the carbonyl carbon. One phenyl ring has two chlorine atoms at the 2nd and 4th positions, while the other phenyl ring has a methyl group at the 4th position. Methanone, (2,4-dichlorophenyl)(4-methylphenyl)- is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its chemical structure, it exhibits potential bioactivity and is of interest in the field of organic chemistry and medicinal chemistry.

5953-02-6

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5953-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5953-02-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5953-02:
(6*5)+(5*9)+(4*5)+(3*3)+(2*0)+(1*2)=106
106 % 10 = 6
So 5953-02-6 is a valid CAS Registry Number.

5953-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dichlorophenyl)-(4-methylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2,4-Dichlor-4'-methyl-benzophenon

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:5953-02-6 SDS

5953-02-6Relevant academic research and scientific papers

Electrophilic Aromatic Substitution. 5. A Kinetic Study of the Friedel-Crafts Acylation in Nitromethane

DeHaan, Franklin P.,Covey, William D.,Delker, Gerald L.,Baker, Nancy J.,Feigon, Juli F.,et al.

, p. 3959 - 3963 (2007/10/02)

Noncompetitive kinetic studies were made of the AlCl3-catalyzed reaction of 2,4-dichlorobenzoyl chloride with benzene and with toluene in nitromethane at 20 deg C.The reaction appears to follow the kinetic expression: rate = (k/0).The kT/kB = 472 +/- 84 and product isomer distribution (8.4 +/- 0.3)percent ortho, (0.43 +/- 0.02)percent meta, and (91.2 +/- 0.3)percent para are in good agreement with the Brown selectivity relationship but unexpectedly indicate a weak rather than strong electrophile.This appears to be an artifact of the inverse rate order dependence upon initial AlCl3 concentration.

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