61348-47-8

Basic information

• Product Name: 2-(5-ISOXAZOLYL)PHENOL
• Synonyms: 5-(2-HYDROXYPHENYL)ISOXAZOLE;2-(ISOXAZOL-5-YL)PHENOL;2-(5-ISOXAZOLYL)PHENOL;2-(5-ISOXAZOLYL)PHENOL 98%;2-(5-Isoxazole)-Phenol;Phenol, 2-(5-isoxazolyl)- (9CI);2-(Isoxazole-5-yl)phenol;6-(2H-1,2-oxazol-5-ylidene)cyclohexa-2,4-dien-1-one
• CAS NO: 61348-47-8
• Molecular Formula: C₉H₇NO₂
• Molecular Weight: 161.16
• Product Categories: OXAZOLE;Building Blocks;Heterocyclic Building Blocks;Isoxazoles
• Mol File: 61348-47-8.mol
• Article Data: 21

Chemical Properties

• Melting Point: 183-186°C
• Boiling Point: 320.88°C at 760 mmHg
• Flash Point: 147.863°C
• Appearance: /
• Density: 1.248g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.582
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-(5-ISOXAZOLYL)PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-ISOXAZOLYL)PHENOL(61348-47-8)
• EPA Substance Registry System: 2-(5-ISOXAZOLYL)PHENOL(61348-47-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 61348-47-8(Hazardous Substances Data)

Usage

General Description

2-(5-ISOXAZOLYL)PHENOL, also known as isoxazolol phenol, is a chemical compound with the molecular formula C9H7NO2. It is a white to off-white crystalline powder with a molecular weight of 161.16 g/mol. 2-(5-ISOXAZOLYL)PHENOL is used in the pharmaceutical industry for its potential biological and medicinal properties. It has been studied for its antimicrobial, antioxidant, and anti-inflammatory properties, and it may have potential applications in the development of drugs for various medical conditions. Additionally, 2-(5-ISOXAZOLYL)PHENOL has also been used in the synthesis of other organic compounds and may have industrial applications.

InChI:InChI=1/C9H7NO2/c11-8-4-2-1-3-7(8)9-5-6-10-12-9/h1-6,11H

Upstream product

• 491-38-3 1-benzopyran-4(4H)-one 
• 39079-62-4 chromone-3-carboxylic acid 
• 67-56-1 methanol 
• 14386-66-4 2-(formylacetyl)phenol 
• 84200-61-3 4-Oxo-4H-<1>benzopyran-3-sulfinsaeure 
• 1776-33-6 3-Diaethylamino-1-<2-hydroxy-phenyl>-propenon 
• 582-24-1 1-phenyl-2-hydroxyethanone 
• 5382-16-1 4-HYDROXYPIPERIDINE 
• 52147-97-4 trans 2-phenylethenesulfonyl chloride 
• 1776-08-5 (E)-3-(dimethylamino)-1-(2-hydroxyphenyl)prop-2-en-1-one 
• 118-93-4 o-hydroxyacetophenone 
• 106129-86-6 1-(2-hydroxyphenyl)-3-dimethylaminoprop-2-enone 
• 66665-80-3 2-hydroxy-ω-formylacetophenone aldoxime 

Downstream Products

• 38518-76-2 2-amino-4H-1-benzopyran-4-one 
• 10523-64-5 2-(5-amino-1H-pyrazol-3-yl)phenol 
• 1380732-85-3 1-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)-2-(2-(isoxazol-5-yl)phenoxy)ethanone 
• 647014-03-7 E-[4-(2-(5-isoxazolyl)phenyloxy)piperidin-1-ylsulphonyl]-2-phenylethene 
• 10523-47-4 3-(2-hydroxyphenyl)-3-oxopropanenitrile 
• 6722-08-3 2-Imino-4-hydroxy-cumarin 
• 65479-00-7 1-acetoxy-2-isoxazol-5-yl-benzene 

Relevant articles and documents

CuI/Cu(OSO2CF3)2 catalysed convenient approach to dichromenopyridines and triazole-thiazole appended chromone derivatives

A variety of new pentacyclic dichromenopyridines have been synthesized from 2-amino chromone and O-propargyloxy salicilaldehydes through intramolecular Povarov reaction using CuI/Cu(OSO2CF3)2 as a Lewis acid catalyst. The

Zn(OTf)2-Catalyzed Formal [3 + 3] Cascade Annulation of Propargylic Alcohols with 2-Aminochromones: Accessing the Chromeno[2,3- b]pyridines

A Zn(OTf)2-catalyzed formal [3 + 3] cascade annulation strategy for the synthesis of functionalized chromeno[2,3-b]pyridines has been developed using propargylic alcohols and 2-aminochromones as the substrates. The protocol provides a convenien

Synthesis of unsymmetrical 4-oxo-2-vinyl-4H-chromene-3-carbonitrile dyes via Knoevenagel reaction

New 4-oxo-2-vinyl-4H-chromene-3-carbonitrile derivatives have been synthesized by the Knoevenagel reaction of 2-methyl-4-oxo-4H-chromene-3-carbonitrile with aromatic and heteroaromatic aldehydes. Spectral properties of the obtained compounds have been studied.