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Benzeneacetic acid, alpha,4-diamino(9CI), also known as 4-Aminophenylacetic acid, is a white crystalline solid chemical compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals and organic compounds. Its significance in the pharmaceutical industry is underscored by its role in the production of drugs such as Candesartan, an angiotensin II receptor antagonist utilized for the treatment of hypertension.

75176-85-1

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75176-85-1 Usage

Uses

Used in Pharmaceutical Industry:
Benzeneacetic acid, alpha,4-diamino(9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of drugs with specific therapeutic effects. Its role in the production of Candesartan highlights its importance in creating medications that address hypertension and related cardiovascular conditions.
Used in Organic Compounds Synthesis:
In addition to its pharmaceutical applications, Benzeneacetic acid, alpha,4-diamino(9CI) is utilized as a building block in the synthesis of other organic compounds, demonstrating its versatility and value in the broader field of organic chemistry.
It is important to handle Benzeneacetic acid, alpha,4-diamino(9CI) with care due to its potential harmful effects if mismanaged, emphasizing the need for proper safety measures during its use in chemical processes and pharmaceutical manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 75176-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75176-85:
(7*7)+(6*5)+(5*1)+(4*7)+(3*6)+(2*8)+(1*5)=151
151 % 10 = 1
So 75176-85-1 is a valid CAS Registry Number.

75176-85-1SDS

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 Benzeneacetic acid, α,4-diamino- (9CI)

1.2 Other means of identification

Product number -
Other names 4-Aminophenylglycine

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:75176-85-1 SDS

75176-85-1Downstream Products

75176-85-1Relevant academic research and scientific papers

Biosynthesis of the Antibiotic Obafluorin from p-Aminophenylalanine and Glycine (Glyoxylate)

Herbert, Richard B.,Knaggs, Andrew R.

, p. 109 - 114 (2007/10/02)

Results of experiments using 'resting' cells of Pseudomonas fluorescens with -, - and 2H2>-glycine as precursors show that glyoxylic acid is specifically the source of C-1 and C-2 of the antibiotic obafluorin 1.The 13C labelling patterns are consistent with the passage of the precursors through the tartronic semialdehyde and glyoxylate pathways.The glycine derivative 6 is not a precursor for 1.The analogues 24 and 25 of p-aminophenylalanine 3 are synthesised and tested as substrates for biosynthesis in P. fluorescens.With 24, the metabolite 26 is detected; no metabolites of 25 are detected.

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.

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