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1-(3-chloro-4-hydroxyphenyl)-2-phenylethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6315-31-7

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6315-31-7 Usage

Chemical structure

The compound consists of a phenyl ring with a chloro and hydroxy group attached at the 3rd and 4th positions, as well as a ketone group attached to the second carbon of a phenylethanone chain.

Molecular weight

Approximately 248.7 g/mol

Appearance

The compound is likely to be a solid or a crystalline substance, although the exact appearance may vary depending on the conditions.

Solubility

The compound may be soluble in organic solvents such as ethanol, methanol, or acetone, but its solubility in water is not specified.

Stability

The compound is expected to be stable under normal conditions, but it may be sensitive to light, heat, or moisture.

Reactivity

The compound may undergo various chemical reactions, such as oxidation, reduction, or substitution, due to the presence of the phenyl ring, chloro group, hydroxy group, and ketone group.

Potential applications

The compound has potential applications in the pharmaceutical and chemical industries due to its unique structure and properties. It may be used as a building block for the synthesis of other compounds or as a starting material for the development of new drugs or pharmaceutical products.

Biological activity

The compound may exhibit biological activity, which could be useful in the development of new drugs or pharmaceutical products. Further research is needed to determine its specific biological properties and potential applications.

Research and development

The specific chemical properties and potential applications of 1-(3-chloro-4-hydroxyphenyl)-2-phenylethanone make it an area of interest for further research and development. This may include exploring its chemical reactivity, investigating its potential applications in the pharmaceutical industry, and studying its biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 6315-31-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6315-31:
(6*6)+(5*3)+(4*1)+(3*5)+(2*3)+(1*1)=77
77 % 10 = 7
So 6315-31-7 is a valid CAS Registry Number.

6315-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chloro-4-hydroxyphenyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names 3'-Chlor-4'-hydroxy-biphenyl-4-carbonsaeure

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:6315-31-7 SDS

6315-31-7Relevant academic research and scientific papers

An improved synthesis of hydroxy aryl ketones by fries rearrangement with methanesulfonic acid/methanesulfonic anhydride

Jeon, Ingyu,Mangion, Ian K.

experimental part, p. 1927 - 1930 (2012/10/08)

Methanesulfonic acid treated with methanesulfonic anhydride effectively mediates the Fries rearrangement of aryl esters to give hydroxy aryl ketones with high yields. Georg Thieme Verlag Stuttgart · New York.

A convenient one-pot completely stereoselective synthesis of trans-4-Hydroxystilbenes and its derivatives and X-ray structure of its precursor

Chhor, Rakeshwar B.,Singh, Kunwar A.,Nosse,Tandon, Vishnu K.

, p. 2519 - 2530 (2007/10/03)

The synthesis of E-isomer of 4-Hydroxystilbene and its derivatives 3 by reductive elimination of the carbonyl function in 2-phenyl-1-(4-hydroxyphenyl)ethan-1-one and its derivatives 2 and the X-ray structure of 2a are described.

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