53519-82-7 Usage
Uses
Used in Pharmaceutical Synthesis:
Amino-(3-Methylphenyl)-acetic acid is used as a key intermediate in the synthesis of pharmaceuticals for its versatile chemical properties and ability to form a variety of drug molecules.
Used in the Production of Antibacterial and Antiviral Drugs:
In the pharmaceutical industry, Amino-(3-Methylphenyl)-acetic acid is used as a precursor in the development of antibacterial and antiviral medications, contributing to the fight against infectious diseases.
Used in the Synthesis of Betahistine:
Amino-(3-Methylphenyl)-acetic acid is used as a building block in the synthesis of betahistine, a medication prescribed for the treatment of vertigo and Ménière's syndrome, highlighting its role in addressing specific medical conditions.
Used in Drug Addiction Treatment:
Amino-(3-Methylphenyl)-acetic acid is studied for its potential use in treating drug addiction, offering a chemical approach to managing substance abuse disorders.
Used in Alcohol Withdrawal Treatment:
AMino-(3-Methylphenyl)-acetic acid is also being investigated for its potential role in alcohol withdrawal treatment, providing a supportive measure in the management of alcohol dependence.
Used in Anti-Inflammatory and Analgesic Applications:
Amino-(3-Methylphenyl)-acetic acid has demonstrated anti-inflammatory and analgesic effects, making it a candidate for use in medications aimed at reducing inflammation and pain.
Check Digit Verification of cas no
The CAS Registry Mumber 53519-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53519-82:
(7*5)+(6*3)+(5*5)+(4*1)+(3*9)+(2*8)+(1*2)=127
127 % 10 = 7
So 53519-82-7 is a valid CAS Registry Number.
53519-82-7Relevant academic research and scientific papers
A facile synthesis of substituted phenylglycines
Davies, Antony J.,Ashwood, Michael S.,Cottrell, Ian F.
, p. 1095 - 1102 (2007/10/03)
A convenient scaleable process for the preparation of substituted phenylglycines 2 by a modified Strecker reaction is described. Bisulfite- mediated addition of benzylamine and cyanide anion to substituted benzaldehydes 3 gave the aminonitriles 4 which were hydrolysed in two steps to the N-protected amino acid 1. Debenzylation using catalytic transfer hydrogenation gave the title compounds in good yield.
7-α-Amino-substituted acylamino-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acids
-
, (2008/06/13)
Certain 7-acylamido-3-(1-carboxy-loweralkyl-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acids and their salts and easily hydrolyzed esters of the 4-carboxyl group were synthesized and found to be potent antibacterial agents which exhibited good aqueous solubility. In a preferred embodiment the 7-substituent was 2'-aminomethylphenylacetamido.
