344598-62-5

Basic information

• Product Name: 2-(2,3-di-p-anisyl-1-oxo-1H-indolizin-7-ylidene)propionaldehyde
• CAS NO: 344598-62-5
• Molecular Weight: 399.446
• Mol File: 344598-62-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2,3-di-p-anisyl-1-oxo-1H-indolizin-7-ylidene)propionaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,3-di-p-anisyl-1-oxo-1H-indolizin-7-ylidene)propionaldehyde(344598-62-5)
• EPA Substance Registry System: 2-(2,3-di-p-anisyl-1-oxo-1H-indolizin-7-ylidene)propionaldehyde(344598-62-5)

Safety Data

• Hazardous Substances Data: 344598-62-5(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 102-69-2 tri-n-propylamine 
• 25361-94-8 2,3-bis(4-methoxyphenyl)cyclopropenone 

Relevant articles and documents

Enamines from Iodine Oxidation of Trialkylamines. 1. Electrophilic Capture by Cationic Heterocyclic Rings

Simple enamines derived from acetaldehyde, acetone, and propionaldehyde were generated in situ by iodine oxidation of triethylamine, N,N-diisopropylmethylamine, and tri-n-propylamine, respectively.The enamines were captured by a variety of cationic substrates including trityl, indolizinium, dithiolium, pyrylium, thiapyrylium, selenapyrylium, and tellapyrylium cations.The use of a second equivalent of iodine (or excess) oxidized the initial products of enamine capture to various iminium dyes.These dyes were easily hydrolyzed to heterocyclylidene aldehydes and ketones.Cyclic amines such as N-methylpyrrolidine gave enamines derived from ring oxidation. 2-Cyano-N,N-dimethylethylamine generated a cyano-substituted enamine under the reaction conditions.