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[3-(2-Fluoro-benzyloxy)-phenyl]-acetic acid is a chemical compound with a molecular formula C16H13FO3. It is a derivative of phenylacetic acid, characterized by the attachment of a fluoro-benzyloxy group to the phenyl ring. [3-(2-FLUORO-BENZYLOXY)-PHENYL]-ACETIC ACID is recognized for its potential therapeutic applications and is valued in the fields of organic synthesis and medicinal chemistry as a building block for the creation of various pharmaceuticals and biologically active molecules. Its unique structure, including the presence of a fluorine atom, can influence its pharmacokinetic and pharmacodynamic properties, positioning it as a significant asset in drug discovery and development.

902837-14-3

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902837-14-3 Usage

Uses

Used in Pharmaceutical and Medicinal Chemistry:
[3-(2-Fluoro-benzyloxy)-phenyl]-acetic acid is utilized as a key building block in the synthesis of pharmaceuticals and biologically active molecules. Its unique structure allows for the development of compounds with specific therapeutic targets and improved pharmacological profiles.
Used in Drug Discovery and Development:
In the realm of drug discovery and development, [3-(2-Fluoro-benzyloxy)-phenyl]-acetic acid serves as a valuable tool. Its fluoro-benzyloxy group can significantly impact the compound's pharmacokinetic and pharmacodynamic properties, leading to the design of more effective and safer drugs.
Used in Anti-inflammatory and Analgesic Applications:
[3-(2-Fluoro-benzyloxy)-phenyl]-acetic acid is being studied for its potential anti-inflammatory and analgesic properties. Its ability to modulate inflammatory responses and alleviate pain makes it a promising candidate for the treatment of various inflammatory and painful conditions.
Used in Organic Synthesis:
In the field of organic synthesis, [3-(2-Fluoro-benzyloxy)-phenyl]-acetic acid is employed as a versatile intermediate for the preparation of a wide range of organic compounds. Its reactivity and structural features facilitate the synthesis of complex organic molecules with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 902837-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,8,3 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 902837-14:
(8*9)+(7*0)+(6*2)+(5*8)+(4*3)+(3*7)+(2*1)+(1*4)=163
163 % 10 = 3
So 902837-14-3 is a valid CAS Registry Number.

902837-14-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H50783)  3-(2-Fluorobenzyloxy)phenylacetic acid, 95%   

  • 902837-14-3

  • 250mg

  • 539.0CNY

  • Detail
  • Alfa Aesar

  • (H50783)  3-(2-Fluorobenzyloxy)phenylacetic acid, 95%   

  • 902837-14-3

  • 1g

  • 2400.0CNY

  • Detail

902837-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-((2-Fluorobenzyl)oxy)phenyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-[3-[(2-fluorophenyl)methoxy]phenyl]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:902837-14-3 SDS

902837-14-3Downstream Products

902837-14-3Relevant academic research and scientific papers

Synthesis and aldose reductase inhibitory activities of novel O-substituted hydroxyphenylacetic acid derivatives

Rakowitz, Dietmar,Angerer, Helga,Matuszczak, Barbara

, p. 547 - 558 (2007/10/03)

In continuation of our work aimed towards the preparation of novel aldose reductase inhibitors, several O-substituted hydroxyphenylacetic acid derivatives were investigated. The highest inhibitory activity was found for compounds 7b and 7c bearing a cyclo

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