80488-98-8

Basic information

• Product Name: 2-(3-bromophenyl)indolizine
• Synonyms: 2-(3-bromophenyl)indolizine
• CAS NO: 80488-98-8
• Molecular Weight: 272.144
• Mol File: 80488-98-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(3-bromophenyl)indolizine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-bromophenyl)indolizine(80488-98-8)
• EPA Substance Registry System: 2-(3-bromophenyl)indolizine(80488-98-8)

Safety Data

• Hazardous Substances Data: 80488-98-8(Hazardous Substances Data)

Upstream product

• 2142-63-4 1-(3-Bromophenyl)ethanone 
• 109-06-8 α-picoline 
• 18523-22-3 2,3'-dibromoacetophenone 

Downstream Products

• 77832-44-1 [2-(3-Bromo-phenyl)-indolizin-3-yl]-(3,5-dibromo-4-hydroxy-phenyl)-methanone 
• 88273-88-5 Toluene-4-sulfonic acid 4-[2-(3-bromo-phenyl)-indolizine-3-carbonyl]-2-chloro-phenyl ester 
• 88273-83-0 Toluene-4-sulfonic acid 2-bromo-4-[2-(3-bromo-phenyl)-indolizine-3-carbonyl]-phenyl ester 
• 79286-16-1 [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3-chloro-4-(3-dibutylamino-propoxy)-phenyl]-methanone; compound with oxalic acid 
• 79286-17-2 [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3-chloro-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid 
• 79285-90-8 [3-Bromo-4-(3-dipropylamino-propoxy)-phenyl]-[2-(3-bromo-phenyl)-indolizin-3-yl]-methanone; compound with oxalic acid 
• 77823-32-6 (3-Bromo-4-hydroxy-phenyl)-[2-(3-bromo-phenyl)-indolizin-3-yl]-methanone 
• 77823-42-8 [2-(3-Bromo-phenyl)-indolizin-3-yl]-(3-chloro-4-hydroxy-phenyl)-methanone 

Relevant articles and documents

A visible-light-induced intermolecular [3 + 2] alkenylation-cyclization strategy: Metal-free construction of pyrrolo[2,1,5-cd] indolizine rings

A simple and efficient visible-light-induced intermolecular [3 + 2] alkenylation-cyclization process has been developed. This reaction provided an unprecedented metal-free double C(sp2)-H bond oxidation coupling of indolizines with electron-deficient alkenes. Through this cascade reaction, a series of pyrrolo[2,1,5-cd]indolizine derivatives with a large π-system were synthesized. Furthermore, this approach features easily available starting materials, good functional group tolerance, step-economy, high efficiency and mild conditions.

Mechanochemical Synthesis of 1,2-Diketoindolizine Derivatives from Indolizines and Epoxides Using Piezoelectric Materials

A simple and efficient mechanochemical-induced approach for the synthesis of 1,2-diketoindolizine derivatives has been developed. BaTiO3 was used as the piezoelectric material in this transformation. This method features no usage of solvent, simple experimental operation, scalable potential, and high conversion efficiency, which make it attractive and practical.

Nitro-para-and meta-substituted 2-phenylindolizines as potential antimicrobial agents

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