7515-38-0

Basic information

• Product Name: (3E)-4-phenylbut-3-en-1-amine
• Synonyms: (3E)-4-Phenylbut-3-en-1-amin; 3-Buten-1-amine, 4-phenyl-, (3E)-
• CAS NO: 7515-38-0
• Molecular Formula: C₁₀H₁₃N
• Molecular Weight: 147.2169
• Mol File: 7515-38-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 263.9°C at 760 mmHg
• Flash Point: 109.7°C
• Density: 0.977g/cm³
• Vapor Pressure: 0.01mmHg at 25°C
• Refractive Index: 1.582
• CAS DataBase Reference: (3E)-4-phenylbut-3-en-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (3E)-4-phenylbut-3-en-1-amine(7515-38-0)
• EPA Substance Registry System: (3E)-4-phenylbut-3-en-1-amine(7515-38-0)

Safety Data

• Hazardous Substances Data: 7515-38-0(Hazardous Substances Data)

Usage

General Description

(3E)-4-phenylbut-3-en-1-amine is a chemical compound with the molecular formula C10H15N. It is an organic compound and an amine, with a phenyl group and a butenyl group attached to the amine functional group. (3E)-4-phenylbut-3-en-1-amine is used in the synthesis of various pharmaceuticals and other organic compounds, and its structure and properties make it suitable for use as an intermediate in organic synthesis. It is also used as a building block in the production of various chemicals and can be used in research and development in the pharmaceutical and chemical industries. Additionally, it may have potential applications in medicinal chemistry and drug discovery. Overall, (3E)-4-phenylbut-3-en-1-amine is an important compound with versatile applications in various fields of chemistry.

Upstream product

• 93652-37-0 4-phenyl-3-butenyl para-toluenesulfonate 
• 100-52-7 benzaldehyde 
• 89996-01-0 (3-aminopropyl)(triphenyl)phosphonium bromide 
• 26121-45-9 (E)-4-phenyl-3-butenamide 
• 85669-63-2 (E)-cinnamyl diethyl phosphate 
• 14371-10-9 (E)-3-phenylpropenal 
• 143741-67-7 N-(4-phenyl-3-butenyl)phthalimide 
• 74592-04-4 (E)-2-(4-phenylbut-3-en-1-yl)isoindoline-1,3-dione 

Downstream Products

• 106814-09-9 N-(E)-(4-phenylbut-3-en-1-yl)acetamide 
• 125630-44-6 3-chloro-propionic acid-(4t-phenyl-but-3-enylamide) 
• 770-36-5 4-phenylbuta-3-en-1-ol 
• 1007-03-0 1-phenyl-1-cyclopropylmethanol 
• 17488-65-2 4-phenylbut-3-en-2-ol 
• 106814-11-3 3-{3-[1-Phenyl-meth-(E)-ylidene]-4,5-dihydro-3H-pyrrol-2-yl}-propionic acid ethyl ester 
• 106814-10-2 N-((E)-4-Phenyl-but-3-enyl)-succinamic acid ethyl ester 
• 125630-52-6 4-{3-[1-Phenyl-meth-(E)-ylidene]-4,5-dihydro-3H-pyrrol-2-yl}-butyric acid ethyl ester 
• 125630-39-9 4-((E)-4-Phenyl-but-3-enylcarbamoyl)-butyric acid ethyl ester 

Relevant articles and documents

Alkene Oxyamination Using Malonoyl Peroxides: Preparation of Pyrrolidines and Isoxazolidines

Treatment of homoallylic N-tosyl amines or allylic N-tosyl hydroxylamines with 1.5 equiv of a malonoyl peroxide provides a stereoselective method to access functionalized pyrrolidines and isoxazolidines. This metal free alkene oxyamination proceeds in 50-

Aza- and oxacarbonylations of allyl phosphates catalyzed by rhodium carbonyl cluster. Selective synthesis of β,γ-unsaturated amides, esters, and acids

Rhodium-catalyzed carbonylation of allyl phosphates under CO (20 atm) at 50 deg C proceeds very efficiently in the presence of amines, alcohols, and water to give the corresponding β,γ-unsaturated amides, esters, and acids, respectively.These carbonylations occur with high regioselectivity at the less substituted carbon of allyl unit to give linear β,υ-unsaturated acid derivatives.