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2-Phenylglyceric acid, also known as 2-phenyl-3-hydroxypropanoic acid, is an organic compound with the chemical formula C9H10O4. It is a chiral molecule, meaning it has two enantiomers: (R)- and (S)-2-phenylglyceric acid. 2-phenylglyceric acid is a derivative of glyceric acid, featuring a phenyl group attached to the second carbon atom. It is a white crystalline solid and is soluble in water, ethanol, and acetone. 2-Phenylglyceric acid has various applications in the pharmaceutical and chemical industries, such as a building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It can also be used as a chiral auxiliary in asymmetric synthesis and as a precursor for the production of various biologically active compounds.

5693-97-0

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5693-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5693-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5693-97:
(6*5)+(5*6)+(4*9)+(3*3)+(2*9)+(1*7)=130
130 % 10 = 0
So 5693-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H15N3O/c21-16(13-10-12(13)11-6-2-1-3-7-11)20-17-18-14-8-4-5-9-15(14)19-17/h1-9,12-13H,10H2,(H2,18,19,20,21)

5693-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Phenylglyceric acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5693-97-0 SDS

5693-97-0Relevant academic research and scientific papers

Dihydroxyacids from the chlorination of ketones: an unexpected process

Guthrie, J. Peter,Cossar, John,Lu, Jinqiao

, p. 1904 - 1908 (2007/10/02)

Chlorination of propiophenone in aqueous alkali at room temperature, with low concentrations of hypochlorite, leads to 2-phenylglyceric acid as the major product.This acid is formed by further oxidation of 1-phenyl-1,2-propanedione, which is an intermediate in the oxidation of propiophenone.Formation of this acid is reasonable in the light of other halogenation chemistry.Analogous reactions are observed for butyrophenone, which yields 2,3-dihydroxy-2-phenylbutanoic acid, and for cycloheptanone, which yields 1,2-dihydroxycyclohexanecarboxylic acid. Key words: 2-phenyl glyceric acid, propiophenone, chlorination, hydrolysis, rearrangement, cycloheptanone, 1,2-dihydroxycyclohexanecarboxylic acid.

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