1003194-36-2

Basic information

• Product Name: exo-[4-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl]acetonitrile
• Synonyms: exo-[4-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl]acetonitrile
• CAS NO: 1003194-36-2
• Molecular Weight: 240.348
• Mol File: 1003194-36-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: exo-[4-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl]acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: exo-[4-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl]acetonitrile(1003194-36-2)
• EPA Substance Registry System: exo-[4-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl]acetonitrile(1003194-36-2)

Safety Data

• Hazardous Substances Data: 1003194-36-2(Hazardous Substances Data)

Upstream product

• 16532-79-9 4-Bromophenylacetonitrile 
• 2292-12-8 3-chloro-8-methyl-8-azabicyclo[3.2.1]octane 
• 120-29-6 3-tropanol 

Relevant articles and documents

Direct aminoalkylation of arenes, heteroarenes, and alkenes via Ni-catalyzed Negishi cross-coupling reactions

A room-temperature Ni-catalyzed cross-coupling of aryl, heteroaryl, and alkenyl electrophiles with aminoalkylzinc bromides, readily available from the corresponding aminoalkyl chlorides via Grignard reagents, was developed. The reaction allows a convenient one-step preparation of various aminoalkyl products, including piperidine and tropane derivatives. Such functionalized amine moieties are widely present in various biologically active molecules. Aryl, heteroaryl, and alkenyl iodides, bromides, chlorides and triflates are suitable electrophiles. A short total synthesis of two natural products, (±)-galipinine and (±)-cusparine, is also reported.