85108-55-0

Basic information

• Product Name: Pyridinium, 2-methyl-1-[(4-nitrophenyl)methyl]-, bromide
• CAS NO: 85108-55-0
• Molecular Formula: C13H13N2O2.Br
• Molecular Weight: 309.162
• Mol File: 85108-55-0.mol

Chemical Properties

• CAS DataBase Reference: Pyridinium, 2-methyl-1-[(4-nitrophenyl)methyl]-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridinium, 2-methyl-1-[(4-nitrophenyl)methyl]-, bromide(85108-55-0)
• EPA Substance Registry System: Pyridinium, 2-methyl-1-[(4-nitrophenyl)methyl]-, bromide(85108-55-0)

Safety Data

• Hazardous Substances Data: 85108-55-0(Hazardous Substances Data)

Upstream product

• 109-06-8 α-picoline 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 100-39-0 benzyl bromide 

Downstream Products

• 76712-19-1 N,N-diethyl-N'-(4-nitro-benzylidene)-p-phenylenediamine 
• 131354-31-9 3-(4-Nitro-phenyl)-[1,3]azaphospholo[1,5-a]pyridine 
• 880177-60-6 3-(4-nitro-phenyl)-2-trifluoromethyl-indolizine 

Relevant articles and documents

An HBT-based fluorescent probe for nitroreductase determination and its application in: Escherichia coli cell imaging

A novel HBT-based fluorescent probe HBTPN was reasonably designed for detecting nitroreductase by merging 4-nitrobenzyl as a sensing moiety to HBT-based dye HBTPP. Experiments showed that probe HBTPN displayed a selective and sensitive "turn-on"response t

Transfer hydrogenation of pyridinium and quinolinium species using ethanol as a hydrogen source to access saturated N-heterocycles

Catalytic transfer hydrogenation (TH) for the reduction of heterocycles is an emerging strategy for accessing biologically active saturated N-heterocycles. Herein, we report a TH protocol that utilizes ethanol as a renewable hydrogen source and an Ir catalyst for the reduction of quinolines and pyridines. The reaction is promoted by simple amides as ligands.

METHOD FOR MODULATING CALCIUM ION-RELEASE-ACTIVATED CALCIUM ION CHANNELS

The invention relates to a method for modulating Ca 2'-release-activated Ca 2+ channels (CRAG) in a cell by administering to the cell a compound of formula (I): or a pharmaceutically acceptable salt, solvate, clathrate, or prodrug thereof wh

2-Methylpyridinium Salts as 1,4-Dinucleophiles. Quinolizinium Salts from the Westphal Condensation

Condensation of 2-methylpyridinium salts with 1,2-dicarbonyls in the presence of base, yielded 2,3-disubstituted quinolizinium compounds.Results obtained with different pyridinium substrates are discussed.