174469-41-1

Basic information

• Product Name: Oxazolo[4,5-b]pyridine, 6-bromo-2-phenyl-
• CAS NO: 174469-41-1
• Molecular Formula: C12H7BrN2O
• Molecular Weight: 275.104
• Mol File: 174469-41-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Oxazolo[4,5-b]pyridine, 6-bromo-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazolo[4,5-b]pyridine, 6-bromo-2-phenyl-(174469-41-1)
• EPA Substance Registry System: Oxazolo[4,5-b]pyridine, 6-bromo-2-phenyl-(174469-41-1)

Safety Data

• Hazardous Substances Data: 174469-41-1(Hazardous Substances Data)

Upstream product

• 21594-52-5 6-bromo-3H-oxazolo[4,5-b]pyridin-2-one 
• 102-96-5 (2-nitroethenyl)benzene 
• 39903-01-0 2-amino-3-hydroxy-5-bromopyridine 
• 65-85-0 benzoic acid 

Downstream Products

• 174469-34-2 6-benzyl-2-phenyloxazolo<4,5-b>pyridine 
• 174469-38-6 (2-phenyloxazolo<4,5-b>pyridin-6-yl)methanoic acid 
• 174469-39-7 (2-phenyloxazolo<4,5-b>pyridin-6-yl)methanoyl chloride 
• 174469-37-5 (2-phenyloxazolo<4,5-b>pyridin-6-yl)carboxaldehyde 
• 174469-35-3 (E)-3-(2-phenyloxazolo<4,5-b>pyridin-6-yl)acrylic acid methyl ester 

Relevant articles and documents

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.

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE

Provided is a novel heterocyclic compound which is useful as a material for an organic electroluminescent device. The heterocyclic compound is represented by the general formula [I]: wherein X represents a nitrogen atom or a carbon atom; Y represents O or S; R1 and R2 each represent, independently of one another, a group selected from the group consisting of a substituted or unsubstituted alkyl group and the like; a represents 0 or more and 3 or less; b represents 0 or more and 3 or less; and Ar1 represents a substituted or unsubstituted heterocyclic ring or the like; and n represents an integer of 2 to 10.