1198612-93-9

Basic information

• Product Name: C₉H₈BrN₃
• CAS NO: 1198612-93-9
• Molecular Weight: 238.087
• Mol File: 1198612-93-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₉H₈BrN₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₉H₈BrN₃(1198612-93-9)
• EPA Substance Registry System: C₉H₈BrN₃(1198612-93-9)

Safety Data

• Hazardous Substances Data: 1198612-93-9(Hazardous Substances Data)

Upstream product

• 5301-96-2 5-(p-C₆H₄CH₃)-1,2,3,-Triazol 
• 59066-81-8 4-(4-methylphenyl)-2H-1,2,3-triazole 
• 33491-05-3 1-(2-bromoethynyl)-4-methylbenzene 

Downstream Products

• 1198613-61-4 C₁₁H₁₂BrN₃ 
• 1198613-63-6 C₁₁H₁₂BrN₃ 
• 1198613-65-8 C₁₁H₁₂BrN₃ 
• 1198613-73-8 C₁₅H₁₈BrN₃O₂ 
• 1198613-77-2 C₁₅H₁₈BrN₃O₂ 
• 1198613-75-0 C₁₅H₁₈BrN₃O₂ 
• 1198613-69-2 C₁₇H₁₆BrN₃ 
• 1198613-71-6 C₁₇H₁₆BrN₃ 
• 1198613-67-0 C₁₇H₁₆BrN₃ 

Relevant articles and documents

Copper-catalyzed synthesis of 4-Aryl-1H-1,2,3-triazoles from 1,1-dibromoalkenes and sodium azide

A new methodology for the Cu-catalyzed synthesis of 1H-1,2,3-triazoles from 1,1-dibromoalkenes and sodium azide is presented. Aryl dibromoolefins were efficiently converted into the corresponding 1,2,3-triazoles. A comprehensive number of functional group

Bromo-directed N-2 alkylation of NH-1,2,3-triazoles: Efficient synthesis of poly-substituted 1,2,3-triazoles

"Chemical Equation Presented" Reaction of 4-bromo-NH-1,2,3- triazoles 2 with alkyl halides In the presence of K2CO3 in DMF produced the corresponding 2-substituted 4-bromo1,2,3-triazoles 5 In a regioselective process. Subsequent Suzuki cross-coupling reaction of these bromides provided an efficient synthesis of 2,4,5-trisubstituted triazoles 3. In addition, reduction of the bromotriazoles by hydrogenation furnished an efficient synthesis of 2,4-disubstituted triazoles 8.