885273-80-3

Basic information

• Product Name: [2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHANOL
• Synonyms: [2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHANOL;2-(4-fluorophenyl)-4-Oxazolemethanol;[2-(4-Fluorophenyl)-1,3-oxazol-4-yl]methanol
• CAS NO: 885273-80-3
• Molecular Formula: C₁₀H₈FNO₂
• Molecular Weight: 193.17
• Mol File: 885273-80-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 339.0±52.0 °C(Predicted)
• Appearance: /
• Density: 1.298±0.06 g/cm3(Predicted)
• PKA: 12.98±0.10(Predicted)
• CAS DataBase Reference: [2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHANOL(885273-80-3)
• EPA Substance Registry System: [2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHANOL(885273-80-3)

Safety Data

• Hazardous Substances Data: 885273-80-3(Hazardous Substances Data)

Usage

General Description

[2-(4-Fluoro-phenyl)-oxazol-4-yl]-methanol is a chemical compound with the molecular formula C11H9FNO2. It is a white crystalline solid that is soluble in organic solvents. [2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHANOL belongs to the oxazole class of molecules and contains a fluorine-substituted phenyl group. It is commonly used in the preparation of pharmaceuticals and agrochemicals due to its potential for biological activity. The presence of the oxazole moiety in the structure suggests that this compound may have some pharmacological properties. However, further research is needed to fully understand its potential uses and effects.

Upstream product

• 916810-62-3 4-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)-2-(4-fluorophenyl)-1,3-oxazole 
• 1314419-49-2 methyl 2-(4-fluorophenyl)-4,5-dihydrooxazole-4-carboxylate 
• 56108-05-5 4-fluorobenzamidic acid methylester hydrochloride salt 
• 1065102-64-8 methyl 2-(4-fluorophenyl)-1,3-oxazole-4-carboxylate 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 22091-39-0 4-Chloromethyl-2-(4-fluorophenyl)oxazole 
• 152940-51-7 2-(4-fluorophenyl)oxazole-4-carbaldehyde 

Relevant articles and documents

Substituted N - ((1 °, 3° - [...] - 4° - yl) - methyl) - 4 - benzoyl piperidine compound and use thereof

The invention discloses a substituted N-((1', 3'-azole-4'-yl)-methyl)-4-benzoyl-hexahydropyridine compound represented by formula I, a preparation method thereof, and applications of the substituted N-((1', 3'-oxazole-4'-yl)-methyl)-4-benzoyl-hexahydropyridine compound in preparation of antituberculous drugs. The substituted N-((1', 3'-azole-4'-yl)-methyl)-4-benzoyl-hexahydropyridine compound possesses activity on mycobacterium tuberculosis-susceptible strains, and also possesses activity on strains with tolerance on traditional first-line antituberculous drugs such as isoniazide and rifampicin, and is a novel mycobacterium tuberculosis resistant compound with a promising application prospect.

COMPOUNDS AND METHODS for the inhibition of HDAC

Disclosed are compounds having the formula: wherein X1, X2, X3, R1, R2, R3, R4, Y, A, Z, L and n are as defined herein, and methods of making and using the same.

Chemical Compounds

This invention relates to non-steroidal compounds that are modulators of androgen, glucocorticoid, mineralocorticoid, and progesterone receptors, and also to the methods for the making and use of such compounds.