52333-44-5

Basic information

• Product Name: Oxazolo[4,5-b]pyridine, 2-phenyl-
• CAS NO: 52333-44-5
• Molecular Formula: C12H8N2O
• Molecular Weight: 196.208
• Mol File: 52333-44-5.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Oxazolo[4,5-b]pyridine, 2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazolo[4,5-b]pyridine, 2-phenyl-(52333-44-5)
• EPA Substance Registry System: Oxazolo[4,5-b]pyridine, 2-phenyl-(52333-44-5)

Safety Data

• Hazardous Substances Data: 52333-44-5(Hazardous Substances Data)

Upstream product

• 16867-03-1 2-amino-3-hydroxypyridine 
• 1663-61-2 triethoxymethylbenzene 
• 100-52-7 benzaldehyde 
• 69634-16-8 N¹-(3-hydroxy-2-pyridyl)benzamide 
• 620939-76-6 N-(3-bromopyridin-2-yl)-2-benzamide 
• 98-88-4 benzoyl chloride 
• 591-50-4 iodobenzene 
• 273-97-2 oxazolo<4,5-b>pyridine 
• 108-86-1 bromobenzene 
• 634202-39-4 N'-(3-hydroxypyridin-2-yl)benzenecarboximidamide 
• 102-96-5 (2-nitroethenyl)benzene 

Downstream Products

• 134377-79-0 2-phenyl-5-butyryloxazolo[4,5-b]pyridine 
• 878805-89-1 7-methyl-2-phenyl[1,3]oxazolo[4,5-b]pyridine 
• 144782-78-5 7-benzoyl-2-phenyloxazolo<4,5-b>pyridine 
• 134377-80-3 7-butyryl-2-phenyloxazolo<4,5-b>pyridine 
• 144782-71-8 7-Bromo-2-phenyl-oxazolo[4,5-b]pyridine 
• 144782-67-2 2-(2-Phenyl-oxazolo[4,5-b]pyridin-7-yl)-propan-2-ol 
• 144782-66-1 1-(2-Phenyl-oxazolo[4,5-b]pyridin-7-yl)-butan-1-ol 
• 144782-65-0 Phenyl-(2-phenyl-oxazolo[4,5-b]pyridin-7-yl)-methanol 
• 144782-68-3 1-(2-Phenyl-oxazolo[4,5-b]pyridin-7-yl)-cyclohexanol 
• 144782-69-4 2-Phenyl-7-trimethylsilanyl-oxazolo[4,5-b]pyridine 
• 144782-70-7 2-Phenyl-oxazolo[4,5-b]pyridine-7-carbaldehyde 

Relevant articles and documents

Unprecedentedly mild direct Pd-catalyzed arylation of oxazolo[4,5-b] pyridine

Pd-catalyzed C-2 arylation of oxazolo[4,5-b]pyridine proceeds efficiently at 30°C and tolerates a variety of aryl halides, including derivatized amino acids for which no racemization was observed during the reaction. Experimental evidence for facile depro

Ce(III)-catalyzed highly efficient synthesis of pyridyl benzamides from aminopyridines and nitroolefins without external oxidants

An efficient synthesis of a variety of pyridyl benzamides from 2-aminopyridines and nitroolefins is described. This rare-earth-metal-catalyzed reaction provides the corresponding products with broad substrate scope in moderate to excellent yields, in the absence of additives and external oxidants. Water is used as the source of the carbonyl oxygen atom in pyridyl benzamides. Furthermore, 2-substituted oxazolo[4,5-b]pyridines are formed in good yields under the standard conditions when 2-aminopyridin-3-ols are used as the substrates.

A green route for the synthesis of 2-substituted benzoxazole derivatives catalyzed by Al3+-exchanged K10 clay

A new, simple, and efficient protocol is developed for the synthesis of 2-substituted benzoxazole derivatives through N-C-O bond formation using Al 3+-exchanged K10 clay (Al3+-K10) as catalyst. A wide range of benzoxazole derivatives