67996-22-9

Basic information

• Product Name: ethyl β-phenyl-1H-indole-3-propionate
• Synonyms: ethyl β-phenyl-1H-indole-3-propionate
• CAS NO: 67996-22-9
• Molecular Weight: 293.365
• Mol File: 67996-22-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl β-phenyl-1H-indole-3-propionate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl β-phenyl-1H-indole-3-propionate(67996-22-9)
• EPA Substance Registry System: ethyl β-phenyl-1H-indole-3-propionate(67996-22-9)

Safety Data

• Hazardous Substances Data: 67996-22-9(Hazardous Substances Data)

Upstream product

• 67996-11-6 5-<1H-indol-3-yl(phenyl)methyl>-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 64-17-5 ethanol 
• 120-72-9 indole 
• 104-55-2 3-phenyl-propenal 
• 5443-49-2 α-bromocinnamaldehyde 
• 100-52-7 benzaldehyde 
• 5292-53-5 diethyl benzalmalonate 
• 185679-93-0 ethyl 2-ethoxycarbonyl-3-(3-indolyl)-3-phenyl propanoate 

Relevant articles and documents

N-Heterocyclic Carbene-Catalyzed β-Indolylation of α-Bromoenals with Indoles

An unprecedented example of NHC-catalyzed β-indolylation of α-bromoenals with indoles has been developed. This concise protocol features several advantages (mild reaction conditions, broad substrate scope) and constructs synthetically useful building blocks, namely β-biaryl methylene esters. Notably, the β-biaryl methylene-type fragment is widely found in natural products or pharmaceuticals. (Figure presented.).

Catalytic enantioselective alkylation of heteroaromatic compounds using alkylidene malonates

A catalytic enantioselective alkylation of heteroaromatic compounds using alkylidene malonates has been developed; the reaction proceeds for different heteroaromatic compounds with alkylidene malonates in high yield and enantiomeric excess.