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Benzoic acid, 4-[([1,1'-biphenyl]-4-ylmethyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61439-49-4

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61439-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61439-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,3 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61439-49:
(7*6)+(6*1)+(5*4)+(4*3)+(3*9)+(2*4)+(1*9)=124
124 % 10 = 4
So 61439-49-4 is a valid CAS Registry Number.

61439-49-4SDS

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 4-[(4-phenylphenyl)methylamino]benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:61439-49-4 SDS

61439-49-4Downstream Products

61439-49-4Relevant academic research and scientific papers

COMPOUNDS AND METHODS FOR MODULATING G PROTEIN-COUPLED RECEPTORS

-

Page/Page column 27; 35, (2008/12/04)

The invention provides methods for modulating G protein-coupled receptor 20 (GPR20), and methods for using such compounds to treat, ameliorate or prevent a condition associated with abnormal or deregulated GPR20.

Potential antiatherosclerotic agents. 2. (Aralkylamino)- and (alkylamino)benzoic acid analogues of cetaben

Albright,DeVries,Largis,Miner,Reich,Schaffer,Shepherd,Upeslacis

, p. 1378 - 1393 (2007/10/02)

The syntheses of a series of (aralkylamino)- and (alkylamino)benzoic acids, as well as the corresponding esters and sodium salts, are described. The compounds were evaluated in vivo in rats for serum sterol and triglyceride lowering activity and in vitro

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