20949-91-1

Basic information

• Product Name: 4-Thiazolecarboxaldehyde, 5-bromo-2-phenyl-
• CAS NO: 20949-91-1
• Molecular Formula: C10H6BrNOS
• Molecular Weight: 268.134
• Mol File: 20949-91-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-Thiazolecarboxaldehyde, 5-bromo-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Thiazolecarboxaldehyde, 5-bromo-2-phenyl-(20949-91-1)
• EPA Substance Registry System: 4-Thiazolecarboxaldehyde, 5-bromo-2-phenyl-(20949-91-1)

Safety Data

• Hazardous Substances Data: 20949-91-1(Hazardous Substances Data)

Upstream product

• 20949-73-9 4-dibromomethyl-2-phenyl-4,5-dihydro-thiazol-4-ol; hydrobromide 
• 23780-13-4 (2-phenylthiazol-4-yl)methanol 
• 4771-31-7 2-phenyl-4-chloromethylthiazole 
• 4771-35-1 5-bromo-4-chloromethyl-2-phenyl-thiazole 
• 221558-23-2 5-bromo-4-dichloromethyl-2-phenylthiazole 
• 20949-90-0 5-bromo-4-dibromomethyl-2-phenyl-thiazole 
• 20949-81-9 2-phenyl-thiazole-4-carbaldehyde 
• 21160-54-3 (5-bromo-2-phenyl-thiazol-4-yl)-methanol 
• 221558-19-6 4-dichloromethyl-2-phenylthiazole 

Downstream Products

• 21160-54-3 (5-bromo-2-phenyl-thiazol-4-yl)-methanol 
• 21160-52-1 5-bromo-2-phenyl-thiazole-4-carboxylic acid 
• 221558-30-1 5-azido-2-phenylthiazole-4-carbaldehyde 
• 116227-94-2 5-Bromo-4-(2,5-diphenyl-3,4-dihydro-2H-pyrazol-3-yl)-2-phenyl-thiazole 
• 116228-04-7 5-Bromo-4-(2,5-diphenyl-2H-pyrazol-3-yl)-2-phenyl-thiazole 
• 116254-18-3 2,3-Dibromo-3-(5-bromo-2-phenyl-thiazol-4-yl)-1-phenyl-propan-1-one 
• 55613-13-3 4-cyano-2-phenyloxazole 
• 221558-33-4 5-azido-2-phenyl-4(N-phenyliminomethyl)thiazole 
• 221558-36-7 4-acetyl-5-azido-2-phenylthiazole 
• 432491-27-5 5-(3-methyl-but-2-enylsulfanyl)-2-phenyl-thiazole-4-carbaldehyde 
• 24641-87-0 5-bromo-2-phenyl-thiazole-4-carbaldehyde acetyl-(4-chloromethyl-thiazol-2-yl)-hydrazone 
• 21160-67-8 4-acetyl-5-bromo-2-phenylthiazole 

Relevant articles and documents

A novel ring transformation of 5-azidothiazoles

The 4-oxoalkyl- and 4-iminoalkyl-5-azidothiazoles undergo a ring transformation with nitrogen loss at relatively low temperatures to afford 4- cyanooxazoles and 4-cyanoimidazoles, respectively. The mechanism, which is thought to involve a ring opening-ring closure process, is discussed.