1380502-88-4

Basic information

• Product Name: (E)-2-(1-phenylprop-1-en-2-yl)-1-(pyrimidin-2-yl)-1H-indole
• Synonyms: (E)-2-(1-phenylprop-1-en-2-yl)-1-(pyrimidin-2-yl)-1H-indole
• CAS NO: 1380502-88-4
• Molecular Weight: 311.386
• Mol File: 1380502-88-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-2-(1-phenylprop-1-en-2-yl)-1-(pyrimidin-2-yl)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(1-phenylprop-1-en-2-yl)-1-(pyrimidin-2-yl)-1H-indole(1380502-88-4)
• EPA Substance Registry System: (E)-2-(1-phenylprop-1-en-2-yl)-1-(pyrimidin-2-yl)-1H-indole(1380502-88-4)

Safety Data

• Hazardous Substances Data: 1380502-88-4(Hazardous Substances Data)

Upstream product

• 673-32-5 1-Phenylprop-1-yne 
• 221044-05-9 N-(2-pyrimidyl)indole 
• 1199-77-5 α-methylcinnamic acid 

Relevant articles and documents

Rh(i)-catalyzed decarbonylative direct C2-olefination of indoles with vinyl carboxylic acids

A general and efficient Rh(i)-catalyzed decarbonylative direct C2-olefination of indoles with vinyl carboxylic acids has been developed. The reaction exhibits excellent functional group tolerance, regioselectivity and stereoselectivity, giving a broad range of C2-alkenylated indoles in good to excellent yields. This journal is

Mild and efficient C2-alkenylation of indoles with alkynes catalyzed by a cobalt complex

Direct alkenylation of the C2-position of indoles bearing an easily removable N-pyrimidyl group with alkynes has been achieved by using a cobalt catalyst complexed with a phosphine-pyridine bidentate ligand. This reaction has wide substrate scope and is highly efficient and stereoselective at room temperature. The alkenylated indoles serve as useful platforms for further synthetic transformations (some products of these transformations are shown in the scheme). Copyright