125209-79-2

Basic information

• Product Name: 3-(2-(2-aminopyridin-3-yl)disulfanyl)pyridin-2-amine
• Synonyms: 3-(2-(2-aminopyridin-3-yl)disulfanyl)pyridin-2-amine;3,3'-Disulfanediylbis(pyridin-2-amine);3-[(2-aminopyridin-3-yl)disulfanyl]pyridin-2-amine;3,3'-Dithiobis[2-pyridinamine]
• CAS NO: 125209-79-2
• Molecular Formula: C10H11N4S2
• Molecular Weight: 251
• Mol File: 125209-79-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-(2-(2-aminopyridin-3-yl)disulfanyl)pyridin-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-(2-aminopyridin-3-yl)disulfanyl)pyridin-2-amine(125209-79-2)
• EPA Substance Registry System: 3-(2-(2-aminopyridin-3-yl)disulfanyl)pyridin-2-amine(125209-79-2)

Safety Data

• Hazardous Substances Data: 125209-79-2(Hazardous Substances Data)

Usage

General Description

3-(2-(2-aminopyridin-3-yl)disulfanyl)pyridin-2-amine is a chemical compound with a complex molecular structure. It contains two pyridine rings, one with an attached amine group and the other with a disulfanyl group. The presence of the disulfanyl group suggests that this compound may have potential applications in organic synthesis, since disulfides are known to undergo a variety of useful chemical reactions. The presence of the amine and pyridine groups also suggests that this compound may have biological activity, since amines and pyridines are commonly found in pharmaceuticals and other biologically active compounds. The synthesis and potential applications of this compound may therefore be of interest to chemists and biochemists alike.

Upstream product

• 110402-20-5 2-aminopyridine-3-thiol 
• 173278-49-4 2-tert-butylthiazolo<4,5-b>pyridine 

Downstream Products

• 110402-20-5 2-aminopyridine-3-thiol 
• 173278-51-8 3-mercapto-2(1H)-pyridinone 

Relevant articles and documents

First synthesis of 3-mercapto-2(1H)-pyridinone, a simple disubstituted pyridine useful for synthesis of the 4-azaphenoxathiine ring system and its novel diazaphenoxathiine analogs: 1,6-Diazaphenoxathiine and 2,6-diazaphenoxathiine

3-Mercapto-2(1H)-pyridinone (1) can be synthesized in three simple high-yielding steps from readily available 2-tert-butylthiazolo[4,5-b]pyridine (2). Its disodium salt condenses with o-chloronitrobenzene, 2-chloro-3-nitropyridine, and 3-chloro-4-nitropyridine 1-oxide to give respectively 4-azaphenoxathiine (10), 1,6-diazaphenoxathiine (12), and 2,6-diazaphenoxathiine 2-oxide (14) which reduces to 2,6-diazaphenoxathiine (15). The structures of these previously unreported azaphenoxathiine systems were confirmed by assignment of their respective 13C NMR spectra.

CARBACEPHEM β-LACTAM ANTIBIOTICS

Carbacephem β-lactam antibiotics having the following chemical structures (I) and (II) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, R1, R2 and R3 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.