1379658-15-7

Basic information

• Product Name: 4-(benzo[d]oxazole-2-carbonyl)benzonitrile
• Synonyms: 4-(benzo[d]oxazole-2-carbonyl)benzonitrile
• CAS NO: 1379658-15-7
• Molecular Weight: 248.241
• Mol File: 1379658-15-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-(benzo[d]oxazole-2-carbonyl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(benzo[d]oxazole-2-carbonyl)benzonitrile(1379658-15-7)
• EPA Substance Registry System: 4-(benzo[d]oxazole-2-carbonyl)benzonitrile(1379658-15-7)

Safety Data

• Hazardous Substances Data: 1379658-15-7(Hazardous Substances Data)

Upstream product

• 1443-80-7 4-cyanophenyl methyl ketone 
• 88-75-5 2-hydroxynitrobenzene 
• 95-55-6 2-amino-phenol 
• 273-53-0 benzoxazole 
• 20099-89-2 4-Cyanophenacyl bromide 
• 1613144-10-7 N-(2-(4-cyanophenyl)-2-oxoethyl)-N-(2-hydroxyphenyl)-4-methylbenzenesulfonamide 
• 3897-39-0 N-(2-hydroxy-phenyl)-toluene-4-sulfonamide 
• 131356-52-0 2,2-dibromo-1-(4-cyanophenyl)ethene 
• 157729-39-0 4-(2-bromoethynyl)-benzonitrile 

Relevant articles and documents

Fe/S-Catalyzed synthesis of 2-benzoylbenzoxazoles and 2-quinolylbenzoxazolesviaredox condensation ofo-nitrophenols with acetophenones and methylquinolines

An Fe/S catalyst generatedin situfrom FeCl2·4H2O and elemental sulfur S8in the presence of a tertiary amine as a base was found to catalyze efficiently a 6e?redox condensation ofo-nitrophenols with acetophenones and methylquinolines. The condensed products 2-benzoylbenzoxazoles and 2-quinolylbenzoxazoles were obtained in reasonable yields with water as the only byproduct at a temperature as low as 80 °C.

Palladium(II)/N-heterocyclic carbene-catalyzed direct C-H acylation of heteroarenes with N-acylsaccharins

N-Acylsaccharin represents a facile acyl group transfer agent to heteroarenes in the presence of Pd(II)/NHC complexes appended with a pyrene unit. Catalytic acylation of heteroarenes was enhanced by the noncovalent interaction between the pyrene unit and

A sustainable synthesis of 2-benzoxazyl and 2-benzothiazyl ketones from alkynyl bromides and 2-amino(thio)phenols promoted by a recyclable catalytic system

An environmentally and economically sustainable synthesis of 2-benzoxazyl ketones and 2-benzothiazyl ketones through FeCl3·6H 2O catalyzed tandem reactions of alkynyl bromides with 2-amino(thio)phenols in [bmim]BF4 has been developed. Remarkable advantages of this new synthetic strategy include high efficiency, readily available starting materials, and recyclable catalyst and reaction medium. An environmentally and economically sustainable synthesis of 2-benzoxazyl ketones and 2-benzothiazyl ketones through FeCl3·6H2O catalyzed tandem reactions of alkynyl bromides with 2-amino(thio)phenols in [bmim]BF4 has been developed. Remarkable advantages of this new synthetic strategy include high efficiency, readily available starting materials, and recyclable catalyst and reaction medium. Copyright