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159503-24-9

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159503-24-9 Usage

Description

4'-Amino-biphenyl-3-carboxylic acid methyl ester, with the molecular formula C14H13NO2, is a methyl ester derivative of 4'-amino-biphenyl-3-carboxylic acid. This chemical compound serves as an intermediate in the synthesis of pharmaceuticals and other organic compounds, known for its improved stability and solubility, making it a valuable asset in both industrial and research applications.

Uses

Used in Pharmaceutical Industry:
4'-Amino-biphenyl-3-carboxylic acid methyl ester is used as a key intermediate in the synthesis of various drugs and medicine formulations, contributing to the development of novel therapeutic agents.
Used in Scientific Research:
As a research chemical, 4'-Amino-biphenyl-3-carboxylic acid methyl ester is utilized in scientific studies and experiments, aiding in the exploration of new chemical reactions and the advancement of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 159503-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,0 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 159503-24:
(8*1)+(7*5)+(6*9)+(5*5)+(4*0)+(3*3)+(2*2)+(1*4)=139
139 % 10 = 9
So 159503-24-9 is a valid CAS Registry Number.

159503-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3'-amino-[1,1'-biphenyl]-4-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 4-(3-aminophenyl)benzoate

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:159503-24-9 SDS

159503-24-9Downstream Products

159503-24-9Relevant articles and documents

Synthesis and biological evaluation of a novel photo-activated histone deacetylase inhibitor

Dear, Anthony E.,Liu, Hongbin,Mountford, Simon,Robinson, Andrea,Sama, Gopal R.,Thompson, Phillip

, (2020/06/05)

Hydroxamic acid-based histone deacetylase inhibitors (HDACi) are a class of epigenetic agents with potentially broad therapeutic application to several disease states including post angioplasty mediated neointimal hyperplasia (NIH). Precise spatiotemporal

Biarylaniline phenethanolamines as potent and selective β3 adrenergic receptor agonists

Uehling, David E.,Shearer, Barry G.,Donaldson, Kelly H.,Chao, Esther Y.,Deaton, David N.,Adkison, Kim K.,Brown, Kathleen K.,Cariello, Neal F.,Faison, Walter L.,Lancaster, Mary E.,Lin, Jasmine,Hart, Robert,Milliken, Tula O.,Paulik, Mark A.,Sherman, Bryan W.,Sugg, Elizabeth E.,Cowan, Conrad

, p. 2758 - 2771 (2007/10/03)

The synthesis of a series of phenethanolamine aniline agonists that contain an aniline ring on the right-hand side of the molecule substituted at the meta position with a benzoic acid or a pyridyl carboxylate is described. Several of the analogues (e.g.,

Palladium-catalyzed coupling of functionalized bromoarenes to a polystyrene-bound aryl tributylstannane

Brody, Marcus S.,Finn

, p. 415 - 418 (2007/10/03)

The Stille reaction with a polystyrene-bound stannyl component, catalyzed by a palladacycle complex, provides a convenient and clean method for the synthesis of substituted biaryls on the resin. Several functional groups useful for the construction of supported polydentate amino alcohols were successfully introduced.

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