18158-72-0

Basic information

• Product Name: Benzenamine, N-ethyl-N-2-propynyl-
• Synonyms: N-Aethyl-N-prop-2-inyl-anilin;Benzenamine,N-ethyl-N-2-propynyl;ethylphenylprop-2-ynylamine;N-ethyl-N-phenyl-N-propargylamine;N-ethyl-N-prop-2-yn-1-ylaniline;N-ethyl-N-propargylaniline;N-ethyl-N-prop-2-ynyl-aniline
• CAS NO: 18158-72-0
• Molecular Formula: C11H13N
• Molecular Weight: 159.231
• Mol File: 18158-72-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 119-120 °C(Press: 15 Torr)
• Density: 0.9922 g/cm3
• CAS DataBase Reference: Benzenamine, N-ethyl-N-2-propynyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-ethyl-N-2-propynyl-(18158-72-0)
• EPA Substance Registry System: Benzenamine, N-ethyl-N-2-propynyl-(18158-72-0)

Safety Data

• Hazardous Substances Data: 18158-72-0(Hazardous Substances Data)

Upstream product

• 103-69-5 N-ethyl-N-phenylamine 
• 106-96-7 propargyl bromide 
• 60256-40-8 N-ethyl-N-(2-bromo-allyl)-aniline 
• 557-20-0 diethylzinc 
• 98-95-3 nitrobenzene 
• 62-53-3 aniline 
• 14465-74-8 N-phenyl-N-prop-2-ynylamine 
• 75-03-6 ethyl iodide 
• 16078-91-4 N-allyl-N-ethylaniline 

Downstream Products

• 58494-59-0 N-ethyl-3-formylindole 
• 1616405-51-6 (E)-N-((1-ethyl-1H-indol-3-yl)methylene)-4-methylbenzenesulfonamide 
• 1616405-43-6 N-ethyl-N-((1-tosyl-1H-1,2,3-triazol-4-yl)methyl)benzenamine 
• 1616405-58-3 (E)-N-((1-ethyl-1H-indol-3-yl)methylene)benzenesulfonamide 
• 1616405-50-5 N-ethyl-N-((1-(phenylsulfonyl)-1H-1,2,3-triazol-4-yl)methyl)aniline 
• 5461-49-4 N-ethylformanilide 
• 133846-57-8 (E)-N-ethyl-N-phenyl-N-(3-ethoxyprop-2-enyl)amine 
• 133846-45-4 (Z)-N-ethyl-N-phenyl-N-(3-ethoxyprop-2-enyl)amine 
• 133846-25-0 N-ethyl-N-phenyl-N-(3-phenylthio-2-phenylsulphinylpropyl)amine 
• 133846-27-2 N-ethyl-N-phenyl-N-(3-ethoxy-2-phenylsulphinylpropyl)amine 
• 136344-47-3 [(5S,6S)-3,9-Bis-(3,5-dichloro-2,4,6-trimethyl-phenyl)-1,7-dioxa-2,8-diaza-spiro[4.4]nona-2,8-dien-6-yl]-ethyl-phenyl-amine 
• 136344-42-8 [3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-4-methylene-4,5-dihydro-isoxazol-5-yl]-ethyl-phenyl-amine 
• 93702-86-4 2-(ethylphenylamino)-2-ethylbenzodioxole 
• 93702-89-7 1-(ethylphenylamino)-1-(2-hydroxyethoxy)-1-propene 

Relevant articles and documents

One-pot facile synthesis, crystal structure and antifungal activity of 1,2,3-triazoles bridged with amine-amide functionalities

A library of twenty five 1,2,3-triazoles bridged with amine-amide functionalities have been synthesized from reaction of N-substituted(prop-2-yn-1-yl)amines (2a–2e), 2-bromo-N-arylacetamides (4a–4e) and sodium azide through copper(I)-catalyzed alkyne-azide cycloaddition. The synthesized compounds were characterized by using FTIR, 1H NMR, 13C NMR, and HRMS techniques. The structures of synthesized 5a (CCDC 1569245) and 5h (CCDC 1569249) were also confirmed by X-ray crystallography. Antifungal evaluation of newly synthesized triazoles was carried out against–Candida albicans and Aspergillus niger. Biological screening of synthesized 1,2,3-triazoles revealed moderate to good antifungal activity against tested strains.

Intramolecular annulation of aromatic rings with N-sulfonyl 1,2,3-triazoles: Divergent synthesis of 3-methylene-2,3-dihydrobenzofurans and 3-methylene-2,3-dihydroindoles

The controllable synthesis of 3-methylene-2,3-dihydrobenzofurans 2 and 3-methylene-2,3-dihydroindoles 5 has been developed through Rh-catalyzed intramolecular annulation of aromatic rings with azavinyl carbenes. This journal is

The Pyrolysis of N-Allyl Compounds: Free-radical and Retro-ene Mechanisms

Flash vacuum pyrolysis of N-alkyl-N-allylanilines gives imines by free radical cleavage of the allyl group followed by loss of an atom (or group of atoms) from the α-carbon atom of the alkyl group.The corresponding N-propargyl derivatives also give imines on pyrolysis, but the mechanism is a concerted retro-ene process which may lead to different products from the corresponding N-allyl compound.N-Allyl-N,N-dialkylamines also decompose thermally by a retro-ene process