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(4-chlorophenyl)(2-hydroxy-3-methylphenyl)methanone, also known as 4-Chloro-3'-methylphenyl phenyl ketone, is a chemical compound with the molecular formula C13H11ClO2. It is a ketone derivative characterized by a phenyl group with a chloro substitution and a hydroxy-methylphenyl group. (4-chlorophenyl)(2-hydroxy-3-methylphenyl)methanone is known for its potential applications across various sectors, including pharmaceuticals, agrochemicals, and organic synthesis, where it serves as an intermediate in the synthesis of biologically active compounds. Furthermore, it is utilized in research and development for its unique chemical properties.

6279-04-5

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6279-04-5 Usage

Uses

Used in Pharmaceutical Applications:
(4-chlorophenyl)(2-hydroxy-3-methylphenyl)methanone is used as an intermediate for the synthesis of various pharmaceutical compounds due to its unique chemical structure and reactivity. It plays a crucial role in the development of new drugs and medicines.
Used in Agrochemical Applications:
In the agrochemical industry, (4-chlorophenyl)(2-hydroxy-3-methylphenyl)methanone is used as a chemical intermediate for the preparation of compounds with pesticidal, herbicidal, or other agricultural benefits, contributing to the enhancement of crop protection and yield.
Used in Organic Synthesis:
(4-chlorophenyl)(2-hydroxy-3-methylphenyl)methanone is utilized as a key intermediate in organic synthesis, allowing for the creation of a wide range of organic compounds with diverse applications, from specialty chemicals to advanced materials.
Used in Research and Development:
(4-chlorophenyl)(2-hydroxy-3-methylphenyl)methanone is also employed in the field of research and development, where it aids scientists in understanding complex chemical reactions and the development of novel chemical processes and products. Its unique properties make it a valuable tool for exploring new avenues in chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 6279-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6279-04:
(6*6)+(5*2)+(4*7)+(3*9)+(2*0)+(1*4)=105
105 % 10 = 5
So 6279-04-5 is a valid CAS Registry Number.

6279-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chlorophenyl)-(2-hydroxy-3-methylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 4'-chloro-2-hydroxy-3-methyl-benzophenone

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:6279-04-5 SDS

6279-04-5Relevant academic research and scientific papers

Efficient catalytic synthesis method of 2-hydroxybenzophenone compound

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Paragraph 0055; 0056, (2019/04/11)

The invention discloses a 2-hydroxybenzophenone compound and a green catalytic synthesis method thereof. According to the method, under the conditions of using coumaranone and coumaranone derivativesas raw materials, using nickel chloride as a catalyst, using methylbenzene as a solvent, using di-tert-butyl peroxide as an oxidizing agent, and using sodium carbonate as alkali, the 2-hydroxybenzophenone compound is obtained at high yield. The method has the advantages that the cost is low; the yield is high; the operation is simple and convenient; no pollution is caused and the like. The potential industrial application prospects are realized. The method provides a cheap and green path for the preparation of the 2-hydroxybenzophenone compound.

Ketone derivatives

-

, (2008/06/13)

o-Hydroxybenzophenones and derivatives thereof are described together with a process for their production. The compounds have anti-allergy activity and are characterized by the presence of an alkyl substituent on the hydroxyphenyl ring.

Potential antiinflammatory compounds. II. Acidic antiinflammatory 1,2-benzisoxazoles

Saunders,Williamson

, p. 1554 - 1558 (2007/10/08)

A number of 1,2-benzisoxazoles, substituted in the 3 position with 4-substituted phenyl groups and in the 5-7 positions with acetic and propionic acid residues, have been synthesized and tested in the rat carrageenan foot edema assay. Activity has been fo

Anti-inflammatory 1,2-benzisoxazole derivatives

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, (2008/06/13)

3-Phenyl substituted 1,2-benzisoxazole acetic and propionic acid derivatives with anti-inflammatory activity.

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