62882-11-5

Basic information

• Product Name: 4-(OXAZOL-2-YL)BENZENAMINE
• Synonyms: 4-(OXAZOL-2-YL)BENZENAMINE;2-(4-Aminophenyl)oxazole, HCl;4-(Oxazol-2-yl)aniline hydrochloride;4-(1,3-oxazol-2-yl)aniline;4-(2-Oxazolyl)benzenamine;4-(Oxazol-2-yl)aniline;1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydro-7-bromoquinoline;1-BOC-7-Bromo-3,4-dihydro-2H-quinoline
• CAS NO: 62882-11-5
• Molecular Formula: C₉H₈N₂O
• Molecular Weight: 160.17
• Mol File: 62882-11-5.mol
• Article Data: 7

Chemical Properties

• Melting Point: 121-123℃
• Boiling Point: 327℃
• Flash Point: 151℃
• Appearance: /
• Density: 1.204
• Storage Temp.: Room temperature.
• PKA: 3.46±0.10(Predicted)
• CAS DataBase Reference: 4-(OXAZOL-2-YL)BENZENAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(OXAZOL-2-YL)BENZENAMINE(62882-11-5)
• EPA Substance Registry System: 4-(OXAZOL-2-YL)BENZENAMINE(62882-11-5)

Safety Data

• Hazardous Substances Data: 62882-11-5(Hazardous Substances Data)

Usage

General Description

4-(Oxazol-2-yl)benzenamine, also known as 2-amino-4-(1,3-oxazol-2-yl)phenol, is an organic compound that belongs to the class of organic compounds known as aminobenzenes. These are benzenes in which one or more hydrogen atoms are replaced by an amino group (NH2). 4-(Oxazol-2-yl)benzenamine has a structure that consists of a Benzene ring substituted by an oxazolyl group on one side and an amino group on the other. It appears as a solid that is probably insoluble in water. As of now, it is primarily used in scientific research, and its toxicity or potential uses are yet unclear due to lack of extensive studies.

Upstream product

• 62882-08-0 2-(p-Nitrophenyl)oxazole 
• 555-16-8 4-nitrobenzaldehdye 
• 391248-21-8 ethyl 2-(4-aminophenyl)oxazole-4-carboxylate 

Downstream Products

• 860542-34-3 N-acetyl-sulfanilic acid-(4-oxazol-2-yl-anilide) 
• 20662-88-8 2-phenyloxazole 
• 68535-42-2 2-hydroxy-5-oxazol-2-yl-benzoic acid 
• 68535-56-8 p-(2-oxazolyl)-phenol 
• 46047-24-9 2-(4-chlorophenyl)oxazole 

Relevant articles and documents

Substituted Oxopyridine Derivatives and Use Thereof in the Treatment of Cardiovascular Disorders

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

SUBSTITUTED OXOPYRIDINE DERIVATIVES AND USE THEREOF IN THE TREATMENT OF CARDIOVASCULAR DISORDERS

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

Palladium-catalyzed direct (hetero)arylation of ethyl oxazole-4- carboxylate: An efficient access to (hetero)aryloxazoles

(Chemical Equation Presented) A straightforward route toward 2-(hetero)arylated and 2,5-di(hetero)arylated oxazoles through regiocontrolled palladium-catalyzed direct (hetero)arylation of ethyl oxazole-4-carboxylate with iodo-, bromo-, and chloro(hetero)a