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(3'-Fluoro-biphenyl-4-yl)-acetic acid is a chemical compound that belongs to the class of biphenyl-4-yl-acetic acids, characterized by the presence of a fluoro substituent at the 3' position. It is a versatile building block in organic synthesis and medicinal chemistry, known for its potential anti-inflammatory and analgesic properties. Its derivatives are of interest in the development of new drugs for treating pain and inflammatory conditions, and it has also been explored for its utility in the synthesis of liquid crystals and materials for organic electronic devices. (3'-Fluoro-biphenyl-4-yl)-acetic acid holds promise for a range of applications across medicine, materials science, and organic chemistry.

5002-38-0

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5002-38-0 Usage

Uses

Used in Pharmaceutical Synthesis:
(3'-Fluoro-biphenyl-4-yl)-acetic acid is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to contribute to the development of new drugs with potential anti-inflammatory and analgesic effects.
Used in Medicinal Chemistry Research:
As a building block, (3'-Fluoro-biphenyl-4-yl)-acetic acid is utilized in medicinal chemistry for the exploration and development of novel therapeutic agents, particularly those targeting pain and inflammatory conditions.
Used in Organic Synthesis:
(3'-Fluoro-biphenyl-4-yl)-acetic acid is employed as a synthetic precursor in organic chemistry, facilitating the creation of a variety of complex organic molecules.
Used in the Development of Liquid Crystals:
In materials science, (3'-Fluoro-biphenyl-4-yl)-acetic acid is used as a component in the synthesis of liquid crystals, which are crucial for the advancement of display technologies and other applications requiring responsive molecular materials.
Used in Organic Electronic Devices:
(3'-Fluoro-biphenyl-4-yl)-acetic acid is also utilized in the synthesis of materials for organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its potential to enhance the performance of these devices.

Check Digit Verification of cas no

The CAS Registry Mumber 5002-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5002-38:
(6*5)+(5*0)+(4*0)+(3*2)+(2*3)+(1*8)=50
50 % 10 = 0
So 5002-38-0 is a valid CAS Registry Number.

5002-38-0SDS

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 2-[4-(3-fluorophenyl)phenyl]acetic acid

1.2 Other means of identification

Product number -
Other names 4-Biphenyl-3'-fluoro-acetic acid

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:5002-38-0 SDS

5002-38-0Relevant academic research and scientific papers

THIAZOLOPIPERAZINE DERIVATIVES AND COMPOSITION FOR PREVENTING OR TREATING AUTOIMMUNE DISEASES COMPRISING THE SAME

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Paragraph 0118-0124; 0131; 0132, (2020/04/01)

The present invention provides a thiazolopiperazine derivative, and a pharmaceutical composition and a health functional food composition for preventing or treating autoimmune diseases containing the same as an active component. A compound represented by chemical formula 1 or a pharmaceutically acceptable salt thereof according to the present invention can have an effect of inhibiting lysophosphatidic acid 1 (LPA1) receptor activation, thereby being able to be usefully used as the pharmaceutical composition or the health functional food composition for preventing or treating LPA1-related diseases. In addition, it is possible to effectively prevent or treat not only autoimmune diseases, but also other immune-related diseases with similar mechanisms of occurrence by using the pharmaceutical composition and the health functional food composition.COPYRIGHT KIPO 2020

Compositions and methods of treating cell proliferation disorders

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Page/Page column 75, (2008/06/13)

The invention relates to compounds and methods for treating cell proliferation disorders.

Aryl-aryl cross coupling on a solid support using zinc organic reagents and palladium catalysis

Marquais, Sophie,Arlt, Michael

, p. 5491 - 5494 (2007/10/03)

Aryl zinc bromides undergo palladium catalyzed coupling reactions to aryl bromides which are bound to a polystyrene resin via an ester linkage. Liberation of the biaryl carboxylic ester was achieved by transesterification.

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