1639441-54-5

Basic information

• Product Name: C₁₇H₁₄BrNO
• Synonyms: C₁₇H₁₄BrNO
• CAS NO: 1639441-54-5
• Molecular Weight: 328.208
• Mol File: 1639441-54-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₇H₁₄BrNO(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₁₄BrNO(1639441-54-5)
• EPA Substance Registry System: C₁₇H₁₄BrNO(1639441-54-5)

Safety Data

• Hazardous Substances Data: 1639441-54-5(Hazardous Substances Data)

Upstream product

• 72053-00-0 1-(4-bromophenyl)-2-(pyridin-2-yl)ethanone 
• 1639441-39-6 C₁₉H₁₈BrNO₄ 

Relevant articles and documents

Direct asymmetric dearomatization of pyridines and pyrazines by iridium-catalyzed allylic amination reactions

The first iridium-catalyzed intramolecular asymmetric allylic dearomatization reaction of pyridines and pyrazines has been realized. 2,3-Dihydroindolizine and 6,7-dihydropyrrolo[1,2-a]pyrazine derivatives were obtained with excellent yields and enantioselectivity. This methodology features dearomatization by direct N-allylic alkylation of pyridines or pyrazines under mild reaction conditions. Getting 'rid' of aromaticity: An iridium-catalyzed intramolecular asymmetric allylic dearomatization reaction converts pyridines and pyrazines (not shown) into 2,3-dihydroindolizine and 6,7-dihydropyrrolo[1,2- a]pyrazine derivatives with excellent yields and enantioselectivities. The dearomatization proceeds by direct N-allylic alkylation of pyridines or pyrazines under mild reaction conditions.