147054-81-7

Basic information

• Product Name: 4-Phenylaminopent-3-en-2-one
• Synonyms: 4-Phenylamino-pent-3-en-2-one;(E)-4-(Phenylamino)-3-penten-2-one;(E)-4-anilinopent-3-en-2-one
• CAS NO: 147054-81-7
• Molecular Formula: C₁₁H₁₃NO
• Molecular Weight: 175.23
• Mol File: 147054-81-7.mol
• Article Data: 51

Chemical Properties

• Boiling Point: 297 ºC
• Flash Point: 121 ºC
• Appearance: /
• Density: 1.059
• Vapor Pressure: 0.00141mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: 4-Phenylaminopent-3-en-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Phenylaminopent-3-en-2-one(147054-81-7)
• EPA Substance Registry System: 4-Phenylaminopent-3-en-2-one(147054-81-7)

Safety Data

• Hazardous Substances Data: 147054-81-7(Hazardous Substances Data)

Usage

General Description

4-Phenylaminopent-3-en-2-one, also known as PAM, is a chemical compound that belongs to the class of aminoketones. It is a yellow to brown crystalline solid with a strong amine odor. PAM is commonly used as an intermediate in organic synthesis and pharmaceutical research. It has also been studied for its potential pharmacological properties, including its effects on the central nervous system. As a chemical reagent, PAM has been used in the synthesis of various pharmaceuticals and other organic compounds due to its unique molecular structure and reactivity. Additionally, PAM has been investigated for its potential use in the development of new medicinal drugs and as a building block for the preparation of various heterocyclic compounds.

InChI:InChI=1/C11H13NO/c1-9(8-10(2)13)12-11-6-4-3-5-7-11/h3-8,12H,1-2H3/b9-8+

Upstream product

• 62-53-3 aniline 
• 123-54-6 acetylacetone 
• 64-10-8 phenyl carbamate 
• 59487-11-5 N-isopropyl-4-amino-3-penten-2-one 
• 16195-91-8 N-cyclohexyl-4-amino-3-penten-2-one 
• 1510707-07-9 C₁₀H₁₇NO 
• 59487-13-7 N-tert-butyl-4-amino-3-penten-2-one 
• 3859-41-4 1,3-cyclopentadione 
• 27363-79-7 2-n-butylthio-2-penten-4-one 

Downstream Products

• 22293-58-9 4-Anilino-3--3-penten-2-on 
• 19164-92-2 2-(phenyl)amino-4-(phenyl)imino-2-pentene 
• 23889-49-8 2-acetyl-3-anilino-but-2-enethioic acid toluene-4-sulfonylamide 
• 83085-35-2 (Z)-4-Phenylamino-3-pyrrolidin-1-ylmethyl-pent-3-en-2-one 
• 104672-43-7 2-Methoxy-6-methyl-4-methylene-3-phenyl-3,4-dihydro-2H-[1,3,2]oxazaphosphinine 
• 83072-64-4 (Z)-3-Dimethylaminomethyl-4-phenylamino-pent-3-en-2-one 
• 83072-86-0 1-(3,6-Dimethyl-1-phenyl-1,2,3,4-tetrahydro-pyrimidin-5-yl)-ethanone 
• 1198-37-4 2,4-dimethylquinoline 
• 84586-45-8 4-methyl-2-[(1E)-2-phenylethenyl]quinoline 

Relevant articles and documents

Packing polymorphism of dicarbonyl-[2-(phenylamino)pent-3-en-4-onato]rhodium(I)

Depending on the crystallization conditions, the interaction between the rhodium metal centres of the separate [Rh(CH3COCHCN(Ph)CH3)(CO)2] molecular units, as described by the interplanar separation and lateral shift of tw

Redox Non-Innocence and Isomer-Specific Oxidative Functionalization of Ruthenium-Coordinated β-Ketoiminate

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Synthesis and coordination chemistry of sterically hindered cobalt(II) β-ketoiminate complexes

The reactions of cobalt(II) chloride with α,β-unsaturated-β-ketoamines, CH3C([dbnd]O)CH[dbnd]C(NHR)CH3, where R = -phenyl, HLPh; R = -mesityl, HLmes; R = -2,6-diisopropylphenyl, HLdipp, and sodium hyd

Metal coordination compound, intermediate, preparation method and application thereof

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A novel and reusable magnetic nanocatalyst developed based on graphene oxide incorporated strontium nanoparticles for the facial synthesis of β-enamino ketones under solvent-free conditions

A novel magnetic SrFeGO nanocatalyst (NC) was synthesized through a simple sol–gel technique by introducing strontium and iron oxide nanoparticles onto graphene. The synthesized NC was characterized using FT-IR and FE-SEM. Subsequently, the catalytic activity of SrFeGO was tested in a reaction between β-dicarbonyl compounds and aniline derivatives to gain β-enamino ketone derivatives under solvent-free conditions. It was found that SrFeGO NC is a potential catalyst for the synthesis of β-enamino ketones. The β-enamino ketone produced by such reactions could be isolated in high purity without the need for chromatographic purifications. The newly prepared magnetic graphene oxide nanocomposite could be recovered and reused for numerous times with no significant decrease in efficiency. Moreover, the protocol has the advantages of excellent yielding (up to 98%) in short a reaction time, benefitting an easy workup procedure and being environmentally friendly.