399559-70-7

Basic information

• Product Name: 4-Penten-1-amine, 2,2-dimethyl-5-phenyl-, (4E)-
• CAS NO: 399559-70-7
• Molecular Formula: C13H19N
• Molecular Weight: 189.301
• Mol File: 399559-70-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 4-Penten-1-amine, 2,2-dimethyl-5-phenyl-, (4E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Penten-1-amine, 2,2-dimethyl-5-phenyl-, (4E)-(399559-70-7)
• EPA Substance Registry System: 4-Penten-1-amine, 2,2-dimethyl-5-phenyl-, (4E)-(399559-70-7)

Safety Data

• Hazardous Substances Data: 399559-70-7(Hazardous Substances Data)

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 87562-50-3 (4E)-2,2-dimethyl-5-phenylpent-4-enenitrile 
• 4392-24-9 Cinnamyl bromide 

Downstream Products

• 1426431-63-1 (E)-2,2-dimethyl-5-phenylpent-4-enylamine-N,N-D₂ 
• 1206670-48-5 2-benzyl-4,4-dimethyl-1-(4-methylbenzenesulfonyl)pyrrolidine 
• 116673-95-1 5-benzyl-3,3-dimethyl-3,4-dihydro-2H-pyrrole 

Relevant articles and documents

C1-symmetric β-Diketiminatoiron(II) Complexes for Hydroamination of Primary Alkenylamines

The synthesis and solid-state characterization of an array of well-defined low-coordinate C1-symmetric β-diketiminatoiron(II) alkyl complexes B3–B6 featuring steric and electronic variations on one of the N-aryl substituen

A novel chiral yttrium complex with a tridentate linked amido-indenyl ligand for intramolecular hydroamination

A new chiral silicon-linked tridentate amido-indenyl ligand was developed from indene and enantiopure 1,2-cyclohexanediamine. Its yttrium complex was synthesized, characterized and applied to efficiently catalyze the intramolecular hydroamination of non-a

Substrate structural effects in yttrium(III)-catalyzed hydroamination/ cyclizations of 1,2-disubstituted and 1,1,2-trisubstituted aminoalkenes terminated by 2-(phenyl) and 2-(2-heteroarenyl) groups

A series of 2-phenyl- and 2-(2-heteroarenyl)-bearing amines possessing 1,2-disubstituted and 1,1,2-trisubststuted alkenes have been evaluated in intramolecular hydroaminations catalyzed by Y[N(TMS)(1. Aminoalkenes possessing a terminal 2-(5-trimethylsilyl)thienyl group exhibited substantially enhanced reactivity compared to their 2-(phenyl)-containing counterparts. Cyclization efficiencies imparted by the 2-[(5-trimethylsilyl)furanyl] substituent were comparable or only slightly better than those obtained with the simple the 2-(phenyl) group. Georg Thieme Verlag Stuttgart · New York.