100191-80-8

Basic information

• Product Name: N-allyl-N-(prop-2-ynyl)benzeneamine
• Synonyms: N-allyl-N-(prop-2-ynyl)benzeneamine
• CAS NO: 100191-80-8
• Molecular Weight: 171.242
• Mol File: 100191-80-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N-allyl-N-(prop-2-ynyl)benzeneamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-allyl-N-(prop-2-ynyl)benzeneamine(100191-80-8)
• EPA Substance Registry System: N-allyl-N-(prop-2-ynyl)benzeneamine(100191-80-8)

Safety Data

• Hazardous Substances Data: 100191-80-8(Hazardous Substances Data)

Upstream product

• 589-09-3 N-allyl-N-phenylamine 
• 106-96-7 propargyl bromide 
• 14465-74-8 N-phenyl-N-prop-2-ynylamine 
• 107-05-1 3-chloroprop-1-ene 
• 62-53-3 aniline 
• 106-95-6 allyl bromide 

Downstream Products

• 93439-98-6 N-phenyl-N-(prop-2-yn-1-yl)cyanamide 
• 109369-02-0 N,N-diallyl-N-prop-2-ynyl-anilinium; bromide 
• 187737-37-7 propene 
• 53146-16-0 tert-butylprop-2-enaldimine 
• 1616405-56-1 (E)-N-((1-allyl-1H-indol-3-yl)methylene)-4-methylbenzenesulfonamide 
• 1616405-48-1 N-allyl-N-((1-tosyl-1H-1,2,3-triazol-4-yl)methyl)aniline 
• 6247-00-3 N,N-diallylaniline 
• 50521-41-0 3,4-bis(methylene)-N-phenyl-azolidine 
• 185384-38-7 2,3-dimethoxy-4-hydroxy-4-[3-(N-allyl-N-phenylamino)-1-propynyl]-2-cyclobuten-1-one 

Relevant articles and documents

Efficient method for the synthesis of chiral pyrrolidine derivatives via ring-closing enyne metathesis reaction

(Chemical Equation Presented) A series of new pyrrolidine derivatives were prepared directly in very good yields, from the substrates containing a basic or nucleophilic N atom via ring-closing enyne metathesis reaction under mild reaction conditions. More

Zinc(ii)-catalyzed intramolecular hydroarylation-redox cross-dehydrogenative coupling of N -propargylanilines with diverse carbon pronucleophiles: Facile access to functionalized tetrahydroquinolines

Zinc(ii)-catalyzed intramolecular hydroarylation-redox cross-dehydrogenative coupling of N-propargylanilines with two types of carbon pronucleophiles (nitromethane as a sp3 carbon pronucleophile and phenylacetylenes as sp carbon pronucleophiles) proceeded to give the 2-substituted tetrahydroquinolines in good yields with 100percent atomic utilization without any additional external oxidants.

Synthesis of substituted 3-indolylimines and indole-3-carboxaldehydes by rhodium(II)-catalyzed annulation

An efficient Cu/Rh-catalyzed method is proposed for the synthesis of 3-indolylimines from N-propargylanilines through Rh(II)-catalyzed denitrogenative annulation of N-sulfonyl-1,2,3-triazoles. Further combined with hydrolysis or reduction, a one-pot method is developed to enable the direct incorporation of an imine, aldehyde, or amine group into an indole system from an alkyne. A variety of substituted 3-indolylimines, indole-3-carboxaldehydes, and 3-Indolylmethanamines are synthesized in good yields.