60011-48-5

Basic information

• Product Name: N-benzyl-N-(3-methyl-2-butyne)aniline
• Synonyms: N-benzyl-N-(3-methyl-2-butyne)aniline
• CAS NO: 60011-48-5
• Molecular Weight: 235.329
• Mol File: 60011-48-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-N-(3-methyl-2-butyne)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N-(3-methyl-2-butyne)aniline(60011-48-5)
• EPA Substance Registry System: N-benzyl-N-(3-methyl-2-butyne)aniline(60011-48-5)

Safety Data

• Hazardous Substances Data: 60011-48-5(Hazardous Substances Data)

Upstream product

• 69611-44-5 N-(3-methyl-2-butyne)aniline 
• 100-39-0 benzyl bromide 
• 62-53-3 aniline 
• 758640-21-0 N-Benzylaniline 
• 3355-28-0 1-Bromo-2-butyne 

Downstream Products

• 17017-60-6 2,3-dimethyl-1-(phenylmethyl)-1H-indole 

Relevant articles and documents

Copper(i)-catalysed intramolecular hydroarylation-redox cross-dehydrogenative coupling ofN-propargylanilines with phosphites

Intramolecular hydroarylation-redox cross-dehydrogenative coupling ofN-propargylanilines with phosphite diesters proceeded in the presence of Cu(i)-catalysts (20 mol%) to selectively give 2-phosphono-1,2,3,4-tetrahydroquinolines in good yields with 100% atomic utilization. P-H and two C-H bonds are activated at once and these hydrogen atoms are trapped by a propargylic triple bond in the molecule.

Rhodium(I)-catalyzed synthesis of indoles: Amino-claisen rearrangement of N-propargylanilines

Mild and facile preparations of 2-substituted or 2,3-disubstituted indole compounds were achieved by RhH(CO)(Ph3P)3 (4-10 mol %)-catalyzed reaction of N-propargylanilines in hexafluoroisopropyl alcohol (HFIP). The formation of indole