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4-Ethoxy-4'-biphenylcarboxylic acid is a chemical compound with the molecular formula C16H14O3, belonging to the class of biphenylcarboxylic acids. It features two aromatic rings connected by a carboxylic acid group, known for its antioxidant and antimicrobial properties, stability, and low toxicity.

729-18-0

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729-18-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Ethoxy-4'-biphenylcarboxylic acid is used as an active ingredient for its antioxidant and antimicrobial properties, contributing to the development of various pharmaceutical formulations.
Used in Agrochemical Industry:
4-Ethoxy-4'-biphenylcarboxylic acid is used as a component in agrochemicals, leveraging its antimicrobial properties to protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
4-Ethoxy-4'-biphenylcarboxylic acid is used as a building block in organic synthesis, taking advantage of its unique chemical structure and reactivity to create new compounds with potential applications in various fields.
Used in Materials Science:
4-Ethoxy-4'-biphenylcarboxylic acid is used in the development of new materials, owing to its potential to contribute to the properties of materials through its chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 729-18-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 729-18:
(5*7)+(4*2)+(3*9)+(2*1)+(1*8)=80
80 % 10 = 0
So 729-18-0 is a valid CAS Registry Number.

729-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-ethoxyphenyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 4'-Aethoxy-biphenyl-4-carbonsaeure

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:729-18-0 SDS

729-18-0Downstream Products

729-18-0Relevant academic research and scientific papers

Identification and initial structure-activity relationships of a novel class of nonpeptide inhibitors of blood coagulation factor Xa

Klein, Scott I.,Czekaj, Mark,Gardner, Charles J.,Guertin, Kevin R.,Cheney, Daniel L.,Spada, Alfred P.,Bolton, Scott A.,Brown, Karen,Colussi, Dennis,Heran, Christopher L.,Morgan, Suzanne R.,Leadley, Robert J.,Dunwiddie, Christopher T.,Perrone, Mark H.,Chu, Valeria

, p. 437 - 450 (2007/10/03)

The discovery and some of the basic structure-activity relationships of a series of novel nonpeptide inhibitors of blood coagulation Factor Xa is described. These inhibitors are functionalized β-alanines, exemplified by 2a. Docking experiments placing 2a in the active site of Factor Xa implied that the most expeditious route to enhancing in vitro potency was to modify the group occupying the S3 site of the enzyme. Increasing the hydrophobic contacts between the inhibitor and the enzyme in this region led to 8, which has served as the prototype for this series. In addition, an enantioselective synthesis of these substituted β-alanines was also developed.

Biphenyl esters and liquid crystalline mixtures comprising them

-

, (2008/06/13)

Biphenyl esters of the formula STR1 wherein X is --CO--O-- or --O--CO-- and R1 and R2 each are alkyl or alkoxy of 1 - 8 carbon atoms, enlarge significantly the temperature range of the nematic phase of liquid-crystalline compositions without adversely affecting other properties.

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