1125-77-5

Usage

Class

Indolizine

Structure

Bicyclic with a five-membered nitrogen-containing ring fused to a six-membered carbon ring

Physical state

Colorless to yellow liquid

Odor

Characteristic

Solubility

Insoluble in water

Usage

Research and laboratory settings as a precursor to various compounds and as a reagent in organic synthesis

Potential applications

Pharmaceutical industry for the development of new drugs

Additional potential uses

Materials science for the creation of advanced materials and coatings

Upstream product

• 100-71-0 2-Ethylpyridine 
• 36944-74-8 1-(1,2-dimethyl-indolizin-3-yl)-ethanone 
• 17624-36-1 2-pyridyllithium 
• 100525-73-3 4-dimethylamino-3-methyl-2-[2]pyridyl-butan-2-ol 
• 78-95-5 chloroacetone 
• 131240-05-6 3-methyl-4-piperidino-2-[2]pyridyl-butan-2-ol 

Downstream Products

• 100931-11-1 3-Aethyl-2-<4-(1,2-dimethyl-indolizin-(3)-yl)-butadien-(1,3)-yl>-benzthiazolium 
• 6768-60-1 bis(1,2-dimethyl-3-indolizinyl)methane 
• 79283-98-0 [3-Bromo-4-(3-dibutylamino-propoxy)-phenyl]-(1,2-dimethyl-indolizin-3-yl)-methanone; compound with oxalic acid 
• 88274-09-3 (3-Bromo-4-hydroxy-phenyl)-(1,2-dimethyl-indolizin-3-yl)-methanone 

Relevant academic research and scientific papers

Palladium-catalyzed addition of nitrogen pronucleophiles to alkylidenecyclopropanes

The inter- and intramolecular additions of cyclic amides (nitrogen pronucleophiles) to methylenecyclopropanes proceeded smoothly in the presence of catalytic amounts of Pd(PPh3)4, affording the corresponding hydroamination products i

Indolizine–Squaraines: NIR Fluorescent Materials with Molecularly Engineered Stokes Shifts

The development of deep red and near infrared emissive materials with high quantum yields is an important challenge. Several classes of squaraine dyes have demonstrated high quantum yields, but require significantly red-shifted absorptions to access the N