23784-49-8

Basic information

• Product Name: N-(2-methylpropyl)-3-phenyl-prop-2-enamide
• Synonyms: N-(2-methylpropyl)-3-phenyl-prop-2-enamide
• CAS NO: 23784-49-8
• Molecular Formula: C₁₃H₁₇NO
• Molecular Weight: 203.2802
• Mol File: 23784-49-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 110-111 °C
• Boiling Point: 378.6°Cat760mmHg
• Flash Point: 227.6°C
• Appearance: /
• Density: 1.002g/cm³
• Vapor Pressure: 6.23E-06mmHg at 25°C
• Refractive Index: 1.546
• PKA: 15.48±0.46(Predicted)
• CAS DataBase Reference: N-(2-methylpropyl)-3-phenyl-prop-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-methylpropyl)-3-phenyl-prop-2-enamide(23784-49-8)
• EPA Substance Registry System: N-(2-methylpropyl)-3-phenyl-prop-2-enamide(23784-49-8)

Safety Data

• Hazardous Substances Data: 23784-49-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H17NO/c1-11(2)10-14-13(15)9-8-12-6-4-3-5-7-12/h3-9,11H,10H2,1-2H3,(H,14,15)

Upstream product

• 112753-90-9 N-cinnamoyl-2,2-dimethylaziridine 
• 126437-19-2 1-cinnamoyl-2,2-dimethylaziridine 
• 201230-82-2 carbon monoxide 
• 78-81-9 isobutylamine 
• 536-74-3 phenylacetylene 

Relevant articles and documents

Enhancing Ligand-Free Fe-Catalyzed Aminocarbonylation of Alkynes by ZrF4

Zirconium fluoride was utilized to promote efficiently iron-catalyzed aminocarbonylation between alkynes and amines without the use of extra ligands. In particular, this new system is applicable to a wide range of amine and alkyne substrates affording α,β-unsaturated amides in good to excellent yields. Preliminary mechanistic studies reveal the activation model involving interactions of ZF4 with both iron catalyst and amine substrates.

Evolutions differentes de radicaux anions formes par voie chimique ou electrochimique

Chemical and electrochemical reductions of N-aroylaziridines 1 are described and compared.The first step is a single electron transfer (1 +e -> 1-. -> 1'-.).But compounds obtained from 1'-. are depending on the method used way followed: chemical reduction of N-cinnamoylaziridine 1e provides pyrrolidone 10e; but oxazoline 11e is available by electrochemical reduction of the same starting material 1e.Counter ion seems responsible of these different results.In agreement with this hypothesis, it is shown that pyrrolidone 10e is obtained from 1j only in presence of a counter ion.

Identification of aliphatic amines from rates of cinnamoylation.

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