70882-08-5

Basic information

• Product Name: N-benzylbuta-2,3-dien-1-amine
• Synonyms: N-benzylbuta-2,3-dien-1-amine
• CAS NO: 70882-08-5
• Molecular Weight: 159.231
• Mol File: 70882-08-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-benzylbuta-2,3-dien-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzylbuta-2,3-dien-1-amine(70882-08-5)
• EPA Substance Registry System: N-benzylbuta-2,3-dien-1-amine(70882-08-5)

Safety Data

• Hazardous Substances Data: 70882-08-5(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 1310558-69-0 N-(buta-2,3-dien-1-yl)benzamide 
• 1197-51-9 N-propargylbenzylamine 
• 100-58-3 phenylmagnesium bromide 
• 85507-12-6 buta-2,3-dien-1-yl methanesulfonate 

Downstream Products

• 1048976-83-5 1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(phenylmethyl)-pyridine 
• 38025-34-2 4-ethyl-1,2,3,6-tetrahydro-1-(phenylmethyl)-pyridine 
• 38025-47-7 1,2,3,6-tetrahydro-4-[(1E)-2-phenylethenyl]-1-(phenylmethyl)-pyridine 
• 13314-69-7 1-benzyl-4-(4-methoxy-phenyl)-1,2,3,6-tetrahydro-pyridine 
• 32245-93-5 1-[4-(1-benzyl-1,2,3,6-tetrahydro-pyridin-4-yl)-phenyl]-ethanone 
• 1301169-85-6 1-benzyl-3-(4-chlorophenyl)-4-(1-p-tolylvinyl)imidazolidin-2-one 
• 1301169-84-5 1-benzyl-3-(4-nitrophenyl)-4-(1-p-tolylvinyl)imidazolidin-2-one 
• 1301169-77-6 1-benzyl-3-phenyl-4-(1-p-tolylvinyl)imidazolidin-2-one 
• 1301169-82-3 1-benzyl-3-(4-methoxylphenyl)-4-(1-p-tolylvinyl)imidazolidin-2-one 
• 1301169-79-8 1,3-dibenzyl-4-(1-(4-methylphenyl)vinyl)imidazolidin-2-one 
• 6913-92-4 1-benzyl-2,5-dihydro-1H-pyrrole 

Relevant articles and documents

A Rare Alder-ene Cycloisomerization of 1,6-Allenynes

Thermally induced cycloisomerization reactions of 1,6-allenynes gives α-methylene-γ-lactams via intramolecular Alder-ene reactions. The mechanism is supported by computational and deuterium labelling studies. This thermal, non-radical method enables the d

Copper(II)-Promoted Cyclization/Difunctionalization of Allenols and Allenylsulfonamides: Synthesis of Heterocycle-Functionalized Vinyl Carboxylate Esters

A unique method to affect intramolecular aminooxygenation and dioxygenation of allenols and allenylsulfonamides is described. These operationally simple reactions occur under neutral or basic conditions where copper(II) carboxylates serve as reaction promoter, oxidant, and carboxylate source. Moderate to high yields of heterocycle-functionalized vinyl carboxylate esters are formed with moderate to high levels of diastereoselectivity. Such vinyl carboxylate esters could serve as precursors to α-amino and α-oxy ketones and derivatives thereof.

Pd-catalyzed asymmetric synthesis of N-allenyl amides and their Au-catalyzed cycloisomerizative hydroalkylation: A new route toward enantioenriched pyrrolidones

Palladium to make them, gold to cyclize them! Gold-catalyzed cycloisomerizative hydroalkylation of N-allenyl amides affords regioselectively 4-vinyl-γ-lactams. This transformation is stereospecific and takes place with a total axis-to-center chirality tra