82746-41-6

Basic information

• Product Name: 1-(2-(4-bromophenyl)-2-oxoethyl)-2-methylpyridinium bromide
• Synonyms: 1-(2-(4-bromophenyl)-2-oxoethyl)-2-methylpyridinium bromide
• CAS NO: 82746-41-6
• Molecular Weight: 371.071
• Mol File: 82746-41-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1-(2-(4-bromophenyl)-2-oxoethyl)-2-methylpyridinium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-(4-bromophenyl)-2-oxoethyl)-2-methylpyridinium bromide(82746-41-6)
• EPA Substance Registry System: 1-(2-(4-bromophenyl)-2-oxoethyl)-2-methylpyridinium bromide(82746-41-6)

Safety Data

• Hazardous Substances Data: 82746-41-6(Hazardous Substances Data)

Upstream product

• 109-06-8 α-picoline 
• 99-73-0 para-bromophenacyl bromide 

Downstream Products

• 255737-16-7 CF₃C(O)OHgCH₂C₅H₄N⁽¹⁺⁾CH₂C(O)C₆H₄Br*Br^(1-)=CF₃C(O)OHgCH₂C₅H₄N(Br)CH₂C(O)C₆H₄Br 
• 255737-24-7 H₃CC₅H₄N⁽¹⁺⁾CH(HgOCOCF₃)C(O)C₆H₄Br*Br^(1-)=[H₃CC₅H₄NCH(HgOCOCF₃)C(O)C₆H₄Br]Br 
• 7496-72-2 2-(4'-bromophenyl)indolizine 

Relevant articles and documents

Synthesis and biological evaluation of some new indolizine derivatives as antitumoral agents

A new series of indolizine derivatives were synthesized and screened for the antiproliferative potential against NCI 60 tumor cell line panel. The results of the study revealed a selective and good antitumor growth inhibitory activity against SNB-75 CNS c

Discovery of indolizines containing triazine moiety as new leads for the development of antitumoral agents targeting mitotic events

Abstract A new family of 3-aroylindolizines bearing a dimethoxytriazine unit in their position 1 was designed, synthesized and evaluated for their ability to inhibit tubulin polymerization and cellular growth in vitro. Compound 39 was the best candidate i

Synthesis, photophysical, and electrochemical properties of 2,5-diaryl-indolizines

A variety of novel 2,5-diaryl-indolizines have been prepared through the palladium-catalyzed cross-coupling reactions of organozinc reagents prepared from 2-aryl-indolizines with aromatic halides. The photophysical properties of representative compounds indicate that the 2,5-diaryl-indolizines are promising candidates to be used in optoelectronic devices and biomolecular labeling. In addition, cyclic voltammetry studies of some nitrophenyl-substituted indolizines have shown evidences of an oxidation process without the correspondent reduction peak suggesting a dimerization reaction.