1417717-41-9

Basic information

• Product Name: 1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-ol
• Synonyms: 1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-ol
• CAS NO: 1417717-41-9
• Molecular Weight: 315.295
• Mol File: 1417717-41-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-ol(1417717-41-9)
• EPA Substance Registry System: 1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-ol(1417717-41-9)

Safety Data

• Hazardous Substances Data: 1417717-41-9(Hazardous Substances Data)

Upstream product

• 14618-45-2 2,2,2-trifluoro-1-(1H-indol-3-yl)ethanone 
• 536-74-3 phenylacetylene 
• 120-72-9 indole 
• 58518-08-4 1,1,1-trifluoro-4-phenylbut-3-yn-2-one 

Downstream Products

• 1417717-70-4 1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbutan-2-ol 
• 1417717-63-5 3,3'-(1,1,1-trifluoro-4-phenylbut-3-yne-2,2-diyl)bis(1H-indole) 
• 1417717-62-4 5-methyl-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole 
• 1417717-64-6 5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole 
• 1417717-65-7 5-bromo-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole 
• 1417717-66-8 methyl 3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole-5-carboxylate 
• 1417717-67-9 3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole-5-carbonitrile 
• 1417717-68-0 2-methyl-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole 
• 1417717-69-1 1-methyl-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole 

Relevant articles and documents

Enantioselective dehydrative γ-arylation of α-indolyl propargylic alcohols with phenols: Access to chiral tetrasubstituted allenes and naphthopyrans

Herein, we report an enantioselective dehydrative γ-arylation of α-indolyl propargylic alcohols with phenols via organocatalysis, which provides efficient access to chiral tetrasubstituted allenes and naphthopyrans in high yields with excellent regio- and