1739-00-0

Basic information

• Product Name: PHENETHYL-PHENYL-AMINE
• Synonyms: PHENETHYL-PHENYL-AMINE;N-Phenethylaniline;N-Phenylbenzeneethanamine;Benzeneethanamine, N-phenyl-;Einecs 217-099-3;N-Phenylbenzeneethaneamine
• CAS NO: 1739-00-0
• Molecular Formula: C₁₄H₁₅N
• Molecular Weight: 197.28
• EINECS: 217-099-3
• Mol File: 1739-00-0.mol
• Article Data: 135

Chemical Properties

• Boiling Point: 353.1 °C at 760 mmHg
• Flash Point: 178.7 °C
• Appearance: /
• Density: 1.06 g/cm³
• Vapor Pressure: 3.67E-05mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: PHENETHYL-PHENYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: PHENETHYL-PHENYL-AMINE(1739-00-0)
• EPA Substance Registry System: PHENETHYL-PHENYL-AMINE(1739-00-0)

Safety Data

• Hazardous Substances Data: 1739-00-0(Hazardous Substances Data)

Usage

General Description

Phenethyl-phenyl-amine, also known as phenethylamine, is a chemical compound with the molecular formula C8H11N. It is a primary amine and is derived from phenethylamine by substitution of a phenyl group for a hydrogen atom. Phenethyl-phenyl-amine is a psychoactive and stimulant compound that is found naturally in the human body and in some plants. It is known for its effects on mood, energy levels, and attention, and has been used as a recreational drug. The compound has also been studied for its potential medical applications, particularly in the treatment of depression and other mood disorders. Additionally, it is a precursor to various other compounds with pharmacological activities.

InChI:InChI=1/C14H15N/c1-3-7-13(8-4-1)11-12-15-14-9-5-2-6-10-14/h1-10,15H,11-12H2

Upstream product

• 854634-81-4 N-phenethyl-toluene-4-sulfonanilide 
• 23052-05-3 N-phenyl-DL-phenylalanine 
• 622-24-2 2-phenylethyl chloride 
• 62-53-3 aniline 
• 100-42-5 styrene 
• 103-63-9 1-phenyl-2-bromoethane 
• 40395-41-3 phenyl-acetic acid-(N,N'-diphenyl-hydrazide) 
• 621-06-7 2,N-diphenylacetamide 
• 38253-22-4 2-(N-phenylethylanilino)cyclohexanone 
• 24760-80-3 2-phenylethyl p-nitrobenzenesulphonate 
• 4455-09-8 2-phenylethyl tosylate 
• 32376-95-7 2-phenylethyl benzenesulphonate 
• 115419-45-9 β-phenylethyldiphenylbismuth 
• 115419-46-0 tris-β-phenylethylbismuth 

Downstream Products

• 102753-63-9 phenethyl-phenyl-carbamic acid-(2-diisopropylamino-ethyl ester) 
• 101113-58-0 N-(2-(cyclohex-1-en-1-yl)ethyl)aniline 
• 76605-81-7 chloro-acetic acid-(N-phenethyl-anilide) 
• 7001-94-7 N-Phenyl-phenaethylcarbaminsaeure-chlorid 
• 96718-77-3 N-Phenethyl-N-phenyl-benzamide 
• 115419-49-3 N-phenyl-N-(2-phenylethyl)aniline 
• 103798-18-1 (2-cyclohex-1-enyl-ethyl)-cyclohexyl-amine 
• 38253-22-4 2-(N-phenylethylanilino)cyclohexanone 
• 13355-47-0 1-phenyl-2-phenyl-1,2,3,4-tetrahydroisoquinoline 
• 96719-09-4 1,2-Diphenyl-3,4-dihydro-isoquinolinium; iodide 
• 96719-83-4 1-Phenethyl-2-phenyl-3,4-dihydro-isoquinolinium; iodide 
• 96719-88-9 1-(β-phenethyl)-2-phenyl-1,2,3,4-tetrahydroisoquinoline 
• 38679-87-7 9-phenethyl-2,3,4,9-tetrahydro-1H-carbazole 
• 640735-03-1 1-phenethyl-indolin-2-one 

Relevant articles and documents

β-phenylethylamines, indolines and isoquinolones via hydroamination of styrenes by microwave irradiation

Microwave irradiation promotes hydroamination of styrenes. This method can be used as a direct way of producing different kinds of bioactive compounds: open chain compounds like β-phenylethylamines or cyclized products like indolines or isoquinolones.

Anti-Markovnikov hydroaminations of styrene catalyzed by palladium(II) N-heterocyclic carbene complexes under conventional and microwave heating

Six palladium(II) complexes with benzimidazole-based N-heterocyclic carbene ligands were synthesized by transmetallation reactions between silver(I) N-heterocyclic carbene complexes and PdCl2(PhCN)2. The complexes were characterized by physicochemical and spectroscopic methods. The palladium complexes were tested as catalysts for intermolecular hydroamination reactions of styrene with various anilines in ionic liquids under both conventional and microwave heating. All of these complexes proved to be catalytically active in these reactions. The anti-Markovnikov addition products were selectively obtained by using 1?mol% of the palladium complex.

Titanium amido- and imido-complexes supported by a tridentate pyrrolyl ligand: Syntheses, characterisation and catalytic activities

The complexes [Ti(NMe2)2(pmpmi)] [H2pmpmi = (2-pyrrolylmethene)-(2-pyrrolylmethyl)imine], [Ti(NtBu)(pmpmi)(py) 2], [Ti(NtBu)(pmpmi)(dpy)] and [Ti(NPh)(pmpmi)(py) 2] have been prepared, characterised and shown to be pre-catalysts for the hydroamination of phenylacetylene with aniline and p-chloroaniline. The X-ray structures of [Ti(NMe2)2(pmpmi)], [Ti(N tBu)(pmpmi)(dpy)] and [Ti(NPh)(pmpmi)(py)2] have been determined.

Two-Step Protocol for Iodotrimethylsilane-Mediated Deoxy-Functionalization of Alcohols

We have developed a two-step protocol for iodotrimethylsilane-mediated deoxy-functionalization of primary and secondary alcohols to afford products containing a C?N, C?S, or C?O bond. In the first step the alcohol undergoes iodination with iodotrimethylsilane, and in the second, the iodine atom is replaced by a N, S, or O nucleophile. Compared with traditional Mitsunobu reaction, non-acidic pre-nucleophiles can be used, and the reaction proceeds with retention of configuration. This operationally simple, highly efficient protocol can be used for some natural products and small-molecule drugs containing hydroxy-group.

A base-free Chan–Lam reaction catalyzed by an easily assembled Cu(II)-carboxylate metal-organic framework

A new copper(II) metal-organic framework is constructed as a sustainable copper heterogeneous catalyst. Cu-DPTCA, with high catalytic activity, can effectively promote the Chan–Lam coupling reaction of arylboronic acids and amines without adding any base or additive.

Photocatalytic one-pot multidirectional N-alkylation over Pt/D-TiO2/Ti3C2: Ti3C2-based short-range directional charge transmission

Visible-light-induced one-pot, multistep, and chemoselectivity adjustable reactions highlight the economical, sustainable, and green process. Herein, we report Pt nanoparticles dispersed on S and N co-doped titanium dioxide/titanium carbide (MXene) (3%Pt/