98055-06-2

Basic information

• Product Name: 1H-Indole, 2-(2-phenylethyl)-
• CAS NO: 98055-06-2
• Molecular Formula: C16H15N
• Molecular Weight: 221.302
• Mol File: 98055-06-2.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 2-(2-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 2-(2-phenylethyl)-(98055-06-2)
• EPA Substance Registry System: 1H-Indole, 2-(2-phenylethyl)-(98055-06-2)

Safety Data

• Hazardous Substances Data: 98055-06-2(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 645-45-4 hydrocinnamic acid chloride 
• 2550-26-7 4-Phenyl-2-butanone 
• 615-43-0 2-iodophenylamine 
• 20845-80-1 1-chloro-4-phenylbutan-2-one 
• 62-53-3 aniline 
• 16520-62-0 4-Phenyl-1-butyne 
• 100-65-2 N-Phenylhydroxylamine 
• 1190425-92-3 (E)-N-(2-pyridylsulfonyl)-2-styrylindole 
• 1035226-00-6 C₁₆H₁₉NO 
• 100-52-7 benzaldehyde 
• 98055-01-7 diethyl-1-phenylsulfonyl-(3-(phenylthio)-indol-2-yl)methylphosphonate 
• 143582-26-7 1-Phenylsulfonyl-2-phenylsulfonylmethyl-3-(phenylthio)indole 
• 143232-22-8 2-phenylthioindole-2-aldehyde 

Downstream Products

• 102552-18-1 dimethyl-[2-(2-phenethyl-indol-3-yl)-ethyl]-amine 
• 103326-39-2 dibenzyl-[2-(2-phenethyl-indol-3-yl)-ethyl]-amine 
• 1609325-60-1 3-benzyl-2-phenethyl-1H-indole 
• 1304141-56-7 (2R,3R)-(-)-2-phenethyl-3-benzylindoline 
• 938326-58-0 2-phenethyl-1H-indole-3-carbonitrile 
• 1357175-02-0 4-methyl-N-((2-phenethyl-1H-indol-3-yl)(phenyl)methyl)benzenesulfonamide 
• 1304141-57-8 (-)-2-phenethyl-3-(cyclohexylmethyl)indoline 
• 916902-82-4 (+)-(R)-2-phenethylindoline 
• 103325-78-6 (2-phenethyl-indol-3-yl)-glyoxylic acid dibenzylamide 
• 102316-66-5 (2-phenethyl-indol-3-yl)-glyoxylic acid dimethylamide 

Relevant articles and documents

Modular counter-Fischer?indole synthesis through radical-enolate coupling

A single-electron transfer mediated modular indole formation reaction from a 2-iodoaniline derivative and a ketone has been developed. This transition-metal-free reaction shows a broad substrate scope and unconventional regioselectivity trends. Moreover, important functional groups for further transformation are tolerated under the reaction conditions. Density functional theory studies reveal that the reaction proceeds by metal coordination, which converts a disfavored 5-endo-trig cyclization to an accessible 7-endo-trig process.

Au-catalyzed synthesis of 2-alkylindoles from N-arylhydroxylamines and terminal alkynes

The first gold-catalyzed addition of N-arylhydroxylamines to aliphatic terminal alkynes is developed to access O-alkenyl-N-arylhydroxylamines, which undergo facile in situ sequential 3,3-rearrangements and cyclodehydrations to afford 2-alkylindoles with regiospecificity and under exceptionally mild reaction conditions.

Palladium(ii)-catalyzed regioselective direct c2 alkenylation of indoles and pyrroles assisted by the n-(2-pyridyl)sulfonyl protecting group

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