62882-08-0

Basic information

• Product Name: 2-(4-NITROPHENYL)OXAZOLE 97
• Synonyms: 2-(4-NITROPHENYL)OXAZOLE 97
• CAS NO: 62882-08-0
• Molecular Formula: C₉H₆N₂O₃
• Molecular Weight: 190.157
• Product Categories: Building Blocks;Heterocyclic Building Blocks;Oxazoles
• Mol File: 62882-08-0.mol
• Article Data: 9

Chemical Properties

• Melting Point: 163.5-164.5 °C
• Boiling Point: 346.23°C at 760 mmHg
• Flash Point: 163.194°C
• Appearance: /
• Density: 1.334g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.585
• Storage Temp.: Room temperature.
• PKA: -0.78±0.10(Predicted)
• CAS DataBase Reference: 2-(4-NITROPHENYL)OXAZOLE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-NITROPHENYL)OXAZOLE 97(62882-08-0)
• EPA Substance Registry System: 2-(4-NITROPHENYL)OXAZOLE 97(62882-08-0)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 62882-08-0(Hazardous Substances Data)

Usage

General Description

2-(4-Nitrophenyl)oxazole 97 is a chemical compound that is commonly used in research and industrial applications. It is a derivative of oxazole, a five-membered aromatic heterocycle containing oxygen and nitrogen atoms. The compound is known for its nitrophenyl group, which makes it a valuable building block for the synthesis of various organic compounds. 2-(4-Nitrophenyl)oxazole 97 is often used as a reagent in organic synthesis and pharmaceutical research, and it is also utilized in the production of agrochemicals and dyes. It is known for its yellow crystalline appearance and is typically sold in a high purity grade of 97% or greater. 2-(4-NITROPHENYL)OXAZOLE 97 has potential value in fields such as pharmaceuticals, materials science, and agrochemical research.

InChI:InChI=1/C9H6N2O3/c12-11(13)8-3-1-7(2-4-8)9-10-5-6-14-9/h1-6H

Upstream product

• 1064706-46-2 2-(4-nitrophenyl)-4,5-dihydro-5-diethylsulfonamideoxazole 
• 636-98-6 p-nitrobenzene iodide 
• 609345-33-7 oxazol-2-ylzinc(II) chloride 
• 586-78-7 para-nitrophenyl bromide 
• 619-72-7 4-nitrobenzonitrile 
• 555-16-8 4-nitrobenzaldehdye 
• 645-36-3 2,2-diethoxy-ethanamine 
• 93-89-0 benzoic acid ethyl ester 
• 18838-10-3 N-(2-hydroxyethyl)-benzamide 
• 7127-19-7 2-phenyl-1,3-oxazoline 
• 122-04-3 4-nitro-benzoyl chloride 
• 7664-93-9 sulfuric acid 
• 20662-88-8 2-phenyloxazole 
• 7465-63-6 2-(4-Nitrophenyl)-4,5-dihydrooxazole 

Downstream Products

• 62882-11-5 4-(1,3-oxazol-2-yl)aniline 
• 860542-34-3 N-acetyl-sulfanilic acid-(4-oxazol-2-yl-anilide) 
• 20662-88-8 2-phenyloxazole 
• 126193-97-3 N-(p-nitrobenzoyl)-1,2,2-trimethoxyethyl amine 

Relevant articles and documents

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.

A versatile synthesis of 2,4-substituted oxazoles

A variety of five-membered ring oxazoles have been synthesised with complete regiocontrol and without the requirement for ring oxidation via a reaction sequence based on a vinyl sulfonamide template. The Royal Society of Chemistry.

An improved method for the palladium cross-coupling reaction of oxazol-2-ylzinc derivatives with aryl bromides

An improved and scalable procedure to couple ozaxole and thiazole to aryl halides has been demonstrated. The required organozinc reagents were prepared from the aryllithium and solid ZnCl2. These reagents have been successfully coupled to a variety of aryl bromides and aryl iodides in good to excellent yields.