252928-81-7

Basic information

• Product Name: 3-(5-oxazolyl)benzonitrile
• Synonyms: 3-(5-oxazolyl)benzonitrile
• CAS NO: 252928-81-7
• Molecular Weight: 170.17
• Mol File: 252928-81-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(5-oxazolyl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(5-oxazolyl)benzonitrile(252928-81-7)
• EPA Substance Registry System: 3-(5-oxazolyl)benzonitrile(252928-81-7)

Safety Data

• Hazardous Substances Data: 252928-81-7(Hazardous Substances Data)

Upstream product

• 6952-59-6 3-cyanobromobenzene 
• 1186127-11-6 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(triisopropylsilyl)-1,3-oxazole 
• 24964-64-5 3-Cyanobenzaldehyde 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 288-42-6 oxazol 

Relevant articles and documents

4-PHENYL-N-(PHENYL)THIAZOL-2-AMINE DERIVATIVES AND RELATED COMPOUNDS AS ARYL HYDROCARBON RECEPTOR (AHR) AGONISTS FOR THE TREATMENT OF E.G. ANGIOGENESIS IMPLICATED OR INFLAMMATORY DISORDERS

4-phenyl-N-(phenyl)thiazol-2-amine and 4-(pyridin-3-yl)-N-( phenyl) thiazol-2-amine derivatives and the corresponding thiadiazole, thiophene, oxazole, oxadiazole, imidazole and triazole derivatives and related compounds as aryl hydrocarbon receptor (AHR) agonists for the treatment of angiogenesis implicated disorders, such as e.g. retinopathy, psoriasis, rheumatoid arthritis, obesity and cancer, or inflammatory disorders.

Improvement of the Van Leusen reaction in the presence of β-cyclodextrin: A green and efficient synthesis of oxazoles in water

An efficient approach for the synthesis of oxazoles through the Van Leusen reaction in the presence of β-cyclodextrin is described. In aqueous medium using β-cyclodextrin as a supramolecular catalyst, tosylmethyl isocyanide was deprotonated by triethylami