104742-05-4

Basic information

• Product Name: Pyridine, 2-[[(4-nitrophenyl)methyl]thio]-
• CAS NO: 104742-05-4
• Molecular Formula: C12H10N2O2S
• Molecular Weight: 246.29
• Mol File: 104742-05-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Pyridine, 2-[[(4-nitrophenyl)methyl]thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 2-[[(4-nitrophenyl)methyl]thio]-(104742-05-4)
• EPA Substance Registry System: Pyridine, 2-[[(4-nitrophenyl)methyl]thio]-(104742-05-4)

Safety Data

• Hazardous Substances Data: 104742-05-4(Hazardous Substances Data)

Upstream product

• 1121-30-8 1-hydroxy-2(1H)-pyridinethione 
• 81779-73-9 chloroxoacetic acid (4-nitrophenyl)methyl ester 
• 3811-73-2 2-mercaptopyridine-1-oxide sodium salt 
• 2637-34-5 2-Sulfanylpyridine 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 619-73-8 4-nitrobenzyl chloride 
• 109-04-6 2-bromo-pyridine 

Downstream Products

• 497850-80-3 7-{4-[2-(butoxy)ethoxy]phenyl}-1-propyl-N-({4-[(2-pyridyl)sulfanyl]methyl}phenyl)-2,3-dihydro-1H-1-benzazepine-4-carboxamide 
• 497851-93-1 4-{[(2-pyridyl)sulfanyl]methyl}aniline 

Relevant articles and documents

Synthesis method of heteroaryl thioether

The invention discloses a synthesis method of heteroaryl thioether. Under the conditions of no catalyst, no solvent, no additive and the like, aryl halide/2-bromopyridine, thiourea and substituted benzyl bromide which are directly taken as raw materials to selectively synthesize asymmetric heteroaryl thioether in one step without using conventional organic sulfides such as mercaptan or thiophenol.The use of organic sulfides with high toxicity and heavy odor, such as mercaptan or thiophenol, is avoided, and the synthesis steps are shortened, so that the synthesis efficiency is improved, the reaction has good selectivity, and the asymmetric thioether can be preferentially obtained.

Orally active CCR5 antagonists as anti-HIV-1 agents. Part 3: Synthesis and biological activities of 1-benzazepine derivatives containing a sulfoxide moiety

In order to develop orally active CCR5 antagonists, 1-propyl- or 1-isobutyl-1-benzazepine derivatives containing a sulfoxide moiety have been designed, synthesized, and evaluated for their biological activities. Sulfoxide compounds containing a 2-pyridyl

Conversion of Hydroxyl Groups in Alcohols to Other Functional Groups with N-Hydroxy-2-thiopyridone, and Its Application to Dialkylamines and Thiols

The radical decarboxylation reaction of N-alkoxyoxalyloxy-2-thiopyridone which was prepared by the reaction of alcohol, oxalyl chloride, and N-hydroxy-2-thiopyridone was studied both in the absence and presence of olefinic compounds.The same reactions with olefinic and acetylenic alcohols gave the corresponding lactone derivatives.On the other hand the unsymmetrical alkyl 2-pyridyl disulfides were obtained by the same reaction with aliphatic thiols.