82593-25-7

Basic information

• Product Name: (E)-4-phenylbut-3-en-1-amine
• Synonyms: (E)-4-phenylbut-3-en-1-amine;4-Phenylbut-3-en-1-aMine
• CAS NO: 82593-25-7
• Molecular Formula: C₁₀H₁₃N
• Molecular Weight: 147.22
• Mol File: 82593-25-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 263.9°C at 760 mmHg
• Flash Point: 109.7°C
• Appearance: /
• Density: 0.977g/cm³
• Vapor Pressure: 0.01mmHg at 25°C
• Refractive Index: 1.582
• CAS DataBase Reference: (E)-4-phenylbut-3-en-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-phenylbut-3-en-1-amine(82593-25-7)
• EPA Substance Registry System: (E)-4-phenylbut-3-en-1-amine(82593-25-7)

Safety Data

• Hazardous Substances Data: 82593-25-7(Hazardous Substances Data)

Usage

General Description

(E)-4-phenylbut-3-en-1-amine, also known as alpha-methylcinnamylamine, is an organic compound with the chemical formula C10H13N. It is a primary amine with a double bond in the carbon chain, giving it a linear structure. (E)-4-phenylbut-3-en-1-amine is often used as a building block in organic synthesis, particularly in the production of pharmaceuticals and other fine chemicals. It is also used in the fragrance industry as a key ingredient in the creation of various scents. (E)-4-phenylbut-3-en-1-amine has a range of applications due to its versatile chemical structure and reactivity.

InChI:InChI=1/C10H13N/c11-9-5-4-8-10-6-2-1-3-7-10/h1-4,6-8H,5,9,11H2/b8-4+

Upstream product

• 143741-67-7 N-(4-phenyl-3-butenyl)phthalimide 
• 10229-11-5 4-phenyl-but-3-yn-1-ol 
• 770-36-5 4-phenylbuta-3-en-1-ol 
• 591-50-4 iodobenzene 

Relevant articles and documents

Directed Nickel-Catalyzed Diastereoselective Reductive Difunctionalization of Alkenyl Amines

We report herein an intermolecular syn-arylalkylation and alkenylalkylation of alkenyl amines with two different organohalides (iodides and bromides) using Ni(II) catalyst. The cleavable bidentate quinolinamide is utilized after extensive directing group screening to enable olefin difunctionalization with high levels of regio-, chemo-, and diastereocontrol. This general and practical protocol is compatible with α- or β-substituted terminal alkenes and internal alkenes, providing rapid access to branched aliphatic amines bearing two skipped and vicinal stereocenters with high diastereoselectivities that would otherwise be difficult to synthesize.