953046-62-3

Basic information

• Product Name: [3-(2-FLUORO-PHENYL)-ISOXAZOL-5-YL]-METHANOL
• Synonyms: [3-(2-FLUORO-PHENYL)-ISOXAZOL-5-YL]-METHANOL;[3-(2-fluorophenyl)-1,2-oxazol-5-yl]Methanol;3-(2-Fluorophenyl)-5-(hydroxymethyl)isoxazole;3-(2-Fluorophenyl)-5-isoxazolemethanol
• CAS NO: 953046-62-3
• Molecular Formula: C₁₀H₈FNO₂
• Molecular Weight: 193.17
• Mol File: 953046-62-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: [3-(2-FLUORO-PHENYL)-ISOXAZOL-5-YL]-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [3-(2-FLUORO-PHENYL)-ISOXAZOL-5-YL]-METHANOL(953046-62-3)
• EPA Substance Registry System: [3-(2-FLUORO-PHENYL)-ISOXAZOL-5-YL]-METHANOL(953046-62-3)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 953046-62-3(Hazardous Substances Data)

Usage

General Description

[3-(2-Fluoro-phenyl)-isoxazol-5-yl]-methanol is a chemical compound that consists of a methanol molecule attached to an isoxazole ring with a 2-fluoro-phenyl substituent. The isoxazole ring contains three carbon atoms, one oxygen atom, and one nitrogen atom, while the methanol molecule consists of a carbon atom bonded to three hydrogen atoms and a hydroxyl group. This chemical may have potential pharmaceutical or biological applications, as isoxazole compounds have been studied for their antimicrobial, antifungal, and anti-inflammatory properties. The fluorine substituent in the phenyl ring could also impart specific properties to the molecule, making it of interest for further research and development in the pharmaceutical industry.

Upstream product

• 24652-66-2 2-fluorobenzaldehyde oxime 
• 107-19-7 propargyl alcohol 
• 446-52-6 2-Fluorobenzaldehyde 

Downstream Products

• 808740-52-5 3-(2-fluorophenyl)isoxazole-5-carbaldehyde 
• 842973-74-4 3-(2-fluorophenyl)isoxazole-5-carboxylic acid 
• 1337539-51-1 C₂₆H₃₁FN₄O 
• 1337539-57-7 C₂₆H₃₀F₂N₄O 
• 1337539-61-3 C₂₆H₃₀ClFN₄O 
• 1337539-65-7 C₂₆H₃₀ClFN₄O 
• 1337539-68-0 C₂₇H₃₃FN₄O₂ 
• 1337539-72-6 C₂₆H₃₀F₂N₄O 
• 1337539-73-7 C₃₃H₃₅F₃N₄O 
• 1337539-74-8 C₂₇H₃₃FN₄O 
• 953046-63-4 1-(3-(2-fluorophenyl)isoxazol-5-yl)methylpiperazine 

Relevant articles and documents

A rapid and efficient solvent-free microwave-assisted synthesis of pyrazolone derivatives containing substituted isoxazole ring

An efficient synthesis of 4-substituted pyrazolone derivatives was developed. 4-Substituted pyrazolone derivatives were synthesized in 78-97% yields starting from various 3-substituted isoxazole-5-carbaldehydes, ethyl acetoacetate and hydrazine under micr

ISOXAZOLE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS

Methods and compounds effective in ameliorating conditions characterized by unwanted calcium channel activity, particularly unwanted N-type or T-type calcium channel activity are disclosed. Specifically, a series of isoxazole containing compounds are disclosed of the general formula (1) where Z is N or CHNR3 and (Ar1)2CR4 is optionally substituted benzhydryl.