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5-(2-Fluorophenyl)nicotinic acid, also known as Fluphacin, is a chemical compound with the molecular formula C12H8FNO2. It is a derivative of nicotinic acid and contains a fluorine-substituted phenyl group. 5-(2-FLUOROPHENYL)NICOTINIC ACID is characterized by its unique structure and properties, making it a valuable tool in pharmaceutical research and development.

705961-96-2

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705961-96-2 Usage

Uses

Used in Pharmaceutical Industry:
5-(2-Fluorophenyl)nicotinic acid is used as a potent and selective agonist for the G-protein-coupled receptor GPR109A. It plays a crucial role in mediating the anti-inflammatory and lipid-lowering effects of niacin, which are beneficial in the treatment of cardiovascular diseases and metabolic disorders.
Used in Cardiovascular Disease Treatment:
5-(2-Fluorophenyl)nicotinic acid is used as a therapeutic agent for cardiovascular diseases. Its agonistic action on the GPR109A receptor helps in reducing inflammation and lowering lipid levels, which are key factors in the development and progression of cardiovascular conditions.
Used in Metabolic Disorder Treatment:
5-(2-Fluorophenyl)nicotinic acid is used as a treatment for metabolic disorders, such as dyslipidemia and insulin resistance. Its ability to modulate the activity of GPR109A receptor contributes to the regulation of lipid metabolism and glucose homeostasis, thereby improving overall metabolic health.
Used in Drug Development:
5-(2-Fluorophenyl)nicotinic acid is used as a lead compound in the development of new drugs targeting the GPR109A receptor. Its structure and properties provide valuable insights into the pharmacological and physiological functions of this receptor, facilitating the design and synthesis of novel therapeutic agents with improved efficacy and safety profiles.
Used in Research:
5-(2-Fluorophenyl)nicotinic acid is used as a research tool for studying the pharmacological and physiological functions of the GPR109A receptor. Its selective agonistic activity allows researchers to investigate the receptor's role in various biological processes, such as inflammation, lipid metabolism, and glucose homeostasis, and to explore its potential as a therapeutic target for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 705961-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,9,6 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 705961-96:
(8*7)+(7*0)+(6*5)+(5*9)+(4*6)+(3*1)+(2*9)+(1*6)=182
182 % 10 = 2
So 705961-96-2 is a valid CAS Registry Number.

705961-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-fluorophenyl)pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-(2-fluorophenyl)-3-pyridinecarboxylic 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:705961-96-2 SDS

705961-96-2Downstream Products

705961-96-2Relevant academic research and scientific papers

A novel phase-switching protecting group for multi-step parallel solution phase synthesis

Li, Xin,Abell, Chris,Congreve, Miles S.,Warrington, Brian H.,Ladlow, Mark

, p. 989 - 998 (2004)

A new phase-tag 1 which facilitates the parallel solution phase synthesis of carboxylic acids, esters, and carboxamides is reported. The new phase tag assists compound purification by enabling the selective resin capture of reaction products in either a reversible pH dependent manner (solid-phase extraction), or irreversibly in a Diels-Alder reaction.

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