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Benzeneacetic acid, α-phenyl, sodium salt, also known as sodium phenylacetate or sodium phenylacetic acid, is a chemical compound with the molecular formula C8H7NaO2. It is a sodium salt derived from benzeneacetic acid, which is an aromatic carboxylic acid. This white crystalline solid is soluble in water and slightly soluble in ethanol. It is primarily used as a pharmaceutical intermediate in the synthesis of various drugs, including anticonvulsants and antidepressants. Sodium phenylacetate is also known for its potential application in the treatment of certain inborn errors of metabolism, such as urea cycle disorders, by promoting the excretion of excess nitrogen in the form of phenylacetylglutamine.

1716-11-6

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1716-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1716-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1716-11:
(6*1)+(5*7)+(4*1)+(3*6)+(2*1)+(1*1)=66
66 % 10 = 6
So 1716-11-6 is a valid CAS Registry Number.

1716-11-6SDS

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 diphenylacetic acid sodium salt

1.2 Other means of identification

Product number -
Other names Natrium-diphenylacetat

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:1716-11-6 SDS

1716-11-6Relevant academic research and scientific papers

Antibacterial activity and structure-activity relationship studies of 4-substituted-5-(diphenylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thiones

Kusmierz, Edyta,Siwek, Agata,Kosikowska, Urszula,Malm, Anna,Stefanska, Joanna,Dzitko, Katarzyna,Wujec, Monika

, p. 95 - 101 (2013/08/22)

Seventeen 4-substituted-5-(diphenylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3- thiones were synthesized and the structures of the compounds were determined by 1H NMR and IR spectra. In vitro antibacterial potency of all title compounds was evaluated. Additionally, the initial in vitro toxicity screening was performed for one compound using the MTT assay technique. A structure-activity relationship (SAR) studies have been carried out to determine the relevance of the different parameters that define the potency of title s-triazoles.

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