143427-56-9

Basic information

• Product Name: Benzenemethanamine, N-3-pentynyl-
• CAS NO: 143427-56-9
• Molecular Formula: C12H15N
• Molecular Weight: 173.258
• Mol File: 143427-56-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenemethanamine, N-3-pentynyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, N-3-pentynyl-(143427-56-9)
• EPA Substance Registry System: Benzenemethanamine, N-3-pentynyl-(143427-56-9)

Safety Data

• Hazardous Substances Data: 143427-56-9(Hazardous Substances Data)

Upstream product

• 3329-88-2 pent-3-yn-1-yl 4-methylbenzenesulfonate 
• 100-46-9 benzylamine 
• 72486-09-0 methanesulfonic acid but-3-ynyl ester 
• 10229-10-4 pent-3-yn-1-ol 
• 106060-18-8 methanesulfonic acid pent-3-ynyl ester 
• 18719-27-2 5-bromo-pent-2-yne 

Downstream Products

• 1258537-90-4 diethyl 2-(benzyl(pent-3-yn-1-yl)amino)malonate 
• 1349835-63-7 (C₆H₅C₆H₄((CH₃)3C)2P)AuCCC₄H₉ 
• 143427-59-2 1-Benzyl-4-iodo-3-methyl-1,2,5,6-tetrahydro-pyridine-2-carboxylic acid ethyl ester 
• 1039627-08-1 C₁₂H₁₇N 

Relevant articles and documents

TETRAHYDROISOQUINOLINE DERIVATIVES

Compounds of Formula (I) are disclosed and methods of treating viral infections with compositions comprising such compounds.

Mechanistic study of gold(I)-catalyzed hydroamination of alkynes: Outer or inner sphere mechanism?

An experimental mechanistic study of the gold(I)-catalyzed hydroamination shows the formation of conformationally flexible auro-iminium salts Au-Im, which originate from the protonation of a vinyl gold species. Rotation around the C-CAu bond is the reason

Zirconocene-mediated synthesis of 3,4-disubstituted piperidines and reduced isoquinolines

Intramolecular cocyclisation of 4-azaocta-1,7-dienes, -1-en-7-ynes, -7- en-1-ynes and -1,7-diynes using 'zirconocene' equivalents affords 3-aza-8- zirconabicyclo[4.3.0]nonanes, -6-enes, -9-enes or -6,9-dienes. Protonolysis, iodinolysis, or carbonylation of these complexes affords 3,4-disubstitued piperidines. Exocyclic 1,3-dienes formed from the coupling/protonolysis of 4- azaocta-1,7-diynes react with activated dienophiles to yield reduced isoquinolines.