52779-56-3

Basic information

• Product Name: CHEMBRDG-BB 4002183
• Synonyms: CHEMBRDG-BB 4002183;(4-FLUOROPHENYL)(PYRIDIN-3-YL)METHANONE;3-[(4-FLUOROPHENYL)CARBONYL]PYRIDINE;(4-fluorophenyl)(pyridin-3-yl)methanone(SALTDATA: FREE);3-(4-Fluorobenzoyl)pyridine
• CAS NO: 52779-56-3
• Molecular Formula: C₁₂H₈FNO
• Molecular Weight: 201.2
• Mol File: 52779-56-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 326.3°C at 760 mmHg
• Flash Point: 151.2°C
• Appearance: /
• Density: 1.219g/cm³
• Vapor Pressure: 0.000217mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: CHEMBRDG-BB 4002183(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 4002183(52779-56-3)
• EPA Substance Registry System: CHEMBRDG-BB 4002183(52779-56-3)

Safety Data

• Hazardous Substances Data: 52779-56-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H8FNO/c13-11-5-3-9(4-6-11)12(15)10-2-1-7-14-8-10/h1-8H

Upstream product

• 10400-19-8 3-pyridinecarbonyl chloride 
• 462-06-6 fluorobenzene 
• 20260-53-1 pyridine-3-carbonyl chloride hydrochloride 

Downstream Products

• 77744-09-3 1-(4-Fluorophenyl)-1-(3-pyridyl)-2-propen-1-ol 
• 328110-68-5 N-hydroxy-1-(4-fluorophenyl)-1-(3-pyridinyl)methanimine 
• 82465-64-3 5-(4-Fluorbenzoyl)-2-pyridincarboxamid 
• 93943-83-0 (E)-7-(4-Fluoro-phenyl)-7-pyridin-3-yl-hept-6-enoic acid 
• 1604834-18-5 C₂₂H₁₉FN₂O 
• 118412-66-1 3-(4-fluorobenzoyl)piperidin-1-ium chloride 
• 52779-69-8 ethyl p-(pyridin-3-ylcarbonyl)hydratropate 
• 52779-70-1 p-(pyridin-3-ylcarbonyl)hydratropic acid hydrochloride 
• 1599530-69-4 (3-(4-(1H-pyrazol-1-yl)benzyl)-4-chloro-2-methoxyquinolin-6-yl)(4-fluorophenyl)(pyridin-3-yl)methanol 
• 52779-62-1 diethyl 2-methyl-2-[p-(pyridin-3-ylcarbonyl)phenyl]malonate 
• 77744-16-2 Acetic acid 1-(4-fluoro-phenyl)-1-pyridin-3-yl-allyl ester 
• 300812-81-1 (4-Fluoro-phenyl)-pyridin-3-yl-methanone O-(2-diethylamino-ethyl)-oxime 
• 295796-20-2 (4-Fluoro-phenyl)-pyridin-3-yl-methanone O-(2-dimethylamino-ethyl)-oxime 

Relevant articles and documents

Diarylmethylidenefuran derivatives, processes for their preparation and their uses in therapeutics

The present invention relates to derivatives of the formula the process for their preparation, and to their uses in therapeutics, especially as drugs with anti-inflammatory, analgesic and chemopreventive properties.

A New Simple Synthesis of Fusaric Acid and Other 5-Alkyl-2-pyridinecarboxylic Acids

Carboxamido groups are introduced into the 6-position of 3-acylpyridines with high regioselectivity via Minisci reaction with formamides, Fe(II) sulfate and tert-butyl hydroperoxide.The isolation procedure is considerably improved by the addition of citric acid for complexation of the Fe ions.Fusaric acid and other 5-alkyl-2-pyridine carboxylic acids are obtained by a following Wolff-Kishner reaction in 20-75percent overall yield.

Aroyl-substituted phenylacetic acid derivatives

Compounds of the class of aroyl-substituted phenylacetic acids and corresponding esters, amides and hydroxamic acids, useful as anti-inflammatory agents and certain novel precursors therefor.