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2-(4-Biphenylyl)-2-hydroxypropionic acid, also known as 2-(4-phenylphenyl)-2-hydroxypropionic acid or simply 4-biphenyl-2-hydroxypropionic acid, is an organic compound with the chemical formula C15H14O3. It is a white crystalline solid that is soluble in water and various organic solvents. 2-(4-Biphenylyl)-2-hydroxypropionic acid is a derivative of hydroxypropionic acid, featuring a biphenyl group (two phenyl rings bonded together) attached to the 2-position of the hydroxypropionic acid backbone. It is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural properties. The compound is also known for its potential applications in the development of new materials and as a building block in the creation of more complex organic molecules.

6244-54-8

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6244-54-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6244-54-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6244-54:
(6*6)+(5*2)+(4*4)+(3*4)+(2*5)+(1*4)=88
88 % 10 = 8
So 6244-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O3/c1-15(17,12-8-4-2-5-9-12)14(16)18-13-10-6-3-7-11-13/h2-11,17H,1H3

6244-54-8SDS

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 phenyl 2-hydroxy-2-phenylpropanoate

1.2 Other means of identification

Product number -
Other names 2-Biphenyl-4-yl-2-hydroxy-propionsaeure

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:6244-54-8 SDS

6244-54-8Relevant academic research and scientific papers

Facile synthesis of α-hydroxy-α-methyl carboxylic acids by electrochemical carboxylation of methyl aryl ketones

Damodar, Janmanchi,Krishna Mohan, Srinivasulu Reddy,Jayarama Reddy, Srinivasulu Reddy

, p. 399 - 402 (2002)

Electrochemical carboxylation of methyl aryl ketones in the presence of atmospheric pressure of carbon dioxide using platinum cathode and dissolved magnesium anode at constant current density of 10 mA/cm2 gave the corresponding α-hydroxy-α-meth

5,5-Disubstituted-3, 4-dihydroxy-2(5H)-furanones and methods of use therefor

-

, (2008/06/13)

The present invention relates to synthetic methods for the production of both optically active and racemic 5,5-disubstituted-3,4-dihydroxy-2(5H)-furanones; 5-[(4-aryl)-3-butynyl]-3,4-dihydroxy-2(5H)-furanones; 5-(2-arylthio)ethyl-3,4-dihydroxy-2(5H)-furanones; and 5-(2-aryloxy)ethyl-3,4-dihydroxy-2(5H)-furanones. This invention further relates to the use of the above mentioned compounds as anti-inflammatory agents through their action as mixed inhibitors of lipid peroxidation, 5-lipoxygenase, cyclooxygenase-1 and cyclooxygenase-2. The invention further relates to the use of such compounds in the treatment of chronic inflammatory disorders such as asthma, rheumatoid arthritis, inflammatory bowel disease, atherosclerosis, acute respiratory distress syndrome, and central nervous system disorders such as Alzheimer's and Parkinson's disease wherein reactive oxygen species and inflammatory mediators are contributing deleterious factors.

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