37664-32-7

Basic information

• Product Name: 2-(1H-1,2,4-triazol-3-ylthio)-1-(4-bromophenyl) ethanone
• Synonyms: 2-(1H-1,2,4-triazol-3-ylthio)-1-(4-bromophenyl) ethanone
• CAS NO: 37664-32-7
• Molecular Weight: 298.163
• Mol File: 37664-32-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(1H-1,2,4-triazol-3-ylthio)-1-(4-bromophenyl) ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1H-1,2,4-triazol-3-ylthio)-1-(4-bromophenyl) ethanone(37664-32-7)
• EPA Substance Registry System: 2-(1H-1,2,4-triazol-3-ylthio)-1-(4-bromophenyl) ethanone(37664-32-7)

Safety Data

• Hazardous Substances Data: 37664-32-7(Hazardous Substances Data)

Upstream product

• 3179-31-5 1H-[1,2,4]triazole-3-thiol 
• 99-73-0 para-bromophenacyl bromide 

Downstream Products

• 37664-01-0 6-(4-bromophenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-90-4 6-(4-bromophenyl)-5-(naphthalen-1-yl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-89-1 6-(4-bromophenyl)-5-(3-fluorophenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-88-0 6-(4-bromophenyl)-5-(2-chlorophenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-86-8 5-(4-tert-butylphenyl)-6-(4-bromophenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-85-7 6-(4-bromophenyl)-5-(4-methoxyphenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-84-6 6-(4-bromophenyl)-5-p-tolylthiazolo[3,2-b]-1,2,4-triazole 
• 1423120-83-5 6-(4-bromophenyl)-5-(4-(trifluoromethyl)phenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-82-4 6-(4-bromophenyl)-5-(4-fluorophenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-81-3 6-(4-bromophenyl)-5-(3-methoxyphenyl)thiazolo[3,2-b]-1,2,4-triazole 
• 1423120-80-2 6-(4-bromophenyl)-5-phenylthiazolo[3,2-b]-1,2,4-triazole 

Relevant articles and documents

Cu-catalyzed direct C-H bond functionalization: A regioselective protocol to 5-aryl thiazolo[3,2-b]-1,2,4-triazoles

An efficient, regioselective C-5 arylation of thiazolo[3,2-b]-1,2,4- triazoles catalyzed by a simple copper catalyst was developed. This arylation proceeded smoothly and tolerated a variety of functional groups (44 examples). A wide range of functionalized thiazolo[3,2-b]-1,2,4-triazole derivatives were obtained in high yields (up to 99% yield). Possible catalytic cycles of the arylation were also discussed.