1043872-04-3

Basic information

• Product Name: (2R,3S)-2-(3,4-dihydroxy-phenyl)-8-[1-(1H-indol-3-yl)-but-3-enyl]-chroman-3,5,7-triol
• Synonyms: (2R,3S)-2-(3,4-dihydroxy-phenyl)-8-[1-(1H-indol-3-yl)-but-3-enyl]-chroman-3,5,7-triol
• CAS NO: 1043872-04-3
• Molecular Weight: 459.499
• Mol File: 1043872-04-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S)-2-(3,4-dihydroxy-phenyl)-8-[1-(1H-indol-3-yl)-but-3-enyl]-chroman-3,5,7-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-2-(3,4-dihydroxy-phenyl)-8-[1-(1H-indol-3-yl)-but-3-enyl]-chroman-3,5,7-triol(1043872-04-3)
• EPA Substance Registry System: (2R,3S)-2-(3,4-dihydroxy-phenyl)-8-[1-(1H-indol-3-yl)-but-3-enyl]-chroman-3,5,7-triol(1043872-04-3)

Safety Data

• Hazardous Substances Data: 1043872-04-3(Hazardous Substances Data)

Upstream product

• 487-89-8 Indole-3-carboxaldehyde 
• 106-95-6 allyl bromide 
• 154-23-4 catechin 

Relevant articles and documents

Three-component indium-mediated domino allylation of 1H-indole-3- carbaldehyde with electron-rich (hetero)arenes: Highly efficient access to variously functionalized indolylbutenes

We have developed a three-component, one-pot domino reaction that combines the allylindation of 1H-indole-3-carbaldehyde with the dehydrative alkylation of stabilized C nucleophiles (e.g., electron-rich heteroarenes, electron-rich aromatics, and stabilized enols) or N nucleophiles (e.g., azoles). Wiley-VCH Verlag GmbH & Co. KGaA, 2008.