1619929-45-1

Basic information

• Product Name: 3-(1-benzyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-1-(furan-2-yl)prop-2-yn-1-one
• Synonyms: 3-(1-benzyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-1-(furan-2-yl)prop-2-yn-1-one
• CAS NO: 1619929-45-1
• Molecular Weight: 329.398
• Mol File: 1619929-45-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(1-benzyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-1-(furan-2-yl)prop-2-yn-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-benzyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-1-(furan-2-yl)prop-2-yn-1-one(1619929-45-1)
• EPA Substance Registry System: 3-(1-benzyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-1-(furan-2-yl)prop-2-yn-1-one(1619929-45-1)

Safety Data

• Hazardous Substances Data: 1619929-45-1(Hazardous Substances Data)

Upstream product

• 1619929-43-9 3-bromo-1-(furan-2-yl)prop-2-yn-1-one 
• 147329-69-9 1-benzyl-1,4,5,6-tetrahydrocyclopentpyrrole 
• 27866-39-3 1-benzyl-4,5,6,7-tetrahydro-1H-indole 

Downstream Products

• 1619929-28-0 3-(1-benzyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-5-(furan-2-yl)-4,5-dihydroisoxazol-5-ol 
• 1619929-33-7 1-benzyl-2-(3-(furan-2-yl)isoxazol-5-yl)-4,5,6,7-tetrahydro-1H-indole 

Relevant articles and documents

Pyrrole–aminopyrimidine ensembles: Cycloaddition of guanidine to acylethynylpyrroles

An efficient method for the synthesis of pharmaceutically prospective pyrrole–aminopyrimidine ensembles (in up to 91% yield) by the cyclocondensation of easily available acylethynylpyrroles with guanidine nitrate has been developed. The reaction proceeds

From 4,5,6,7-tetrahydroindoles to 3- or 5-(4,5,6,7-tetrahydroindol-2-yl) isoxazoles in two steps: A regioselective switch between 3- and 5-isomers

(4,5,6,7-Tetrahydroindol-2-yl)alkynes, synthesized by cross-coupling of 4,5,6,7-tetrahydroindoles with aroyl(hetaroyl)bromoalkynes or ethyl bromopropynoate in the presence of K2CO3, regioselectively cyclize with hydroxylamine to eith