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3-(2-hydroxy-5-methyl-phenyl)-3-phenyl-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73779-10-9

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73779-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73779-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,7 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73779-10:
(7*7)+(6*3)+(5*7)+(4*7)+(3*9)+(2*1)+(1*0)=159
159 % 10 = 9
So 73779-10-9 is a valid CAS Registry Number.

73779-10-9SDS

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 3-(2-hydroxy-5-methyl-phenyl)-3-phenyl-propionic acid

1.2 Other means of identification

Product number -
Other names 3-(2-Hydroxy-5-methyl-phenyl)-3-phenyl-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:73779-10-9 SDS

73779-10-9Relevant academic research and scientific papers

p-Toluenesulfonic acid mediated hydroarylation of cinnamic acids with anisoles and phenols under metal and solvent-free conditions

Jagdale, Arun R.,Sudalai, Arumugam

, p. 4895 - 4898 (2008/02/08)

Hydroarylation of cinnamic acids with anisoles and phenols mediated by p-toluenesulfonic acid (p-TSA) under metal and solvent-free conditions gave 3-(4-methoxyphenyl)-3-phenylpropanoic acids and dihydrocoumarins, respectively, in high yields and excellent selectivity.

ENANTIOSELECTIVE SYNTHESIS OF ENANTIOMERICALLY ENRICHED COMPOUNDS

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Page/Page column 9; 10, (2010/02/10)

Method of preparing an enantiomerically enriched compound of formula (II) comprising enantioselective hydrogenation of a compound of general formula (I): where W, X and Z have the meanings indicated in the description, to give a compound of general formula (II): where W, Y, T and C* have the meanings indicated in the description, in the presence of a catalyst or its suitable precursor based on Rh, Ru or Ir, having an oxidation state of 0, +1 or +2, and containing at least one enantiomerically enriched chiral ligand.

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