CAS 2127-10-8

2,2′-Dithiobis[5-nitropyridine]

Description:

2,2′-Dithiobis[5-nitropyridine] is an organic compound characterized by its dithiobis structure, which features two 5-nitropyridine moieties linked by a disulfide bond. This compound is notable for its yellow crystalline appearance and is soluble in organic solvents, making it useful in various chemical applications. The presence of nitro groups on the pyridine rings contributes to its electron-withdrawing properties, enhancing its reactivity in nucleophilic substitution reactions. Additionally, the disulfide linkage provides the compound with unique redox properties, allowing it to participate in oxidation-reduction reactions. 2,2′-Dithiobis[5-nitropyridine] is often utilized in the synthesis of more complex molecules and can serve as a reagent in the development of sensors or catalysts. Its stability under ambient conditions and the ability to form derivatives make it a valuable compound in both research and industrial applications. Safety precautions should be observed when handling this compound due to its potential toxicity and reactivity.

Formula: C₁₀H₆N₄O₄S₂

InChI: InChI=1S/C10H6N4O4S2/c15-13(16)7-1-3-9(11-5-7)19-20-10-4-2-8(6-12-10)14(17)18/h1-6H

InChI key: InChIKey=ROUFCTKIILEETD-UHFFFAOYSA-N

SMILES: N(=O)(=O)C=1C=CC(SSC2=CC=C(N(=O)=O)C=N2)=NC1

Synonyms:

• Bis(5-nitro-2-pyridyl) disulfide
• 2,2′-Dithiobis(5-nitropyridine)
• 2,2′-Dithiobis[5-nitropyridine]
• Pyridine, 2,2′-dithiobis[5-nitro-
• DTNP

1,2-Bis(5-nitropyridin-2-yl)disulfane

CAS: 2127-10-8

Formula: C₁₀H₆N₄O₄S₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 310.3090

Ref: IN-DA003DC9

2,2'-Dithiobis(5-nitropyridine)

CAS: 2127-10-8

2,2'-Dithiobis(5-nitropyridine)

Formula: C₁₀H₆N₄O₄S₂

Purity: 98%

Color and Shape: brown solid

Molecular weight: 310.31g/mol

Ref: 54-OR902011

2,2'-Dithio-bis(5-nitropyridine)

CAS: 2127-10-8

2,2'-Dithio-bis(5-nitrophenyl) is a redox probe that can be used to study ATP-sensitive K+ channels. This probe has been shown to bind to the carboxy terminal of the channel and disulfide bond through its thiol group. The binding of 2,2'-dithio-bis(5-nitropyridine) to the activated liver cells causes an increase in the redox potential, which leads to an accumulation of electrons in these cells. These electrons are then transferred to pyridine nucleotides and phosphate ions, leading to an increase in ATP levels and activation of ATP-sensitive K+ channels.

Formula: C₁₀H₆N₄O₄S₂

Purity: Min. 95%

Molecular weight: 310.31 g/mol

Ref: 3D-FD49852

2,2′-Dithiobis(5-nitropyridine)

CAS: 2127-10-8

Formula: C₁₀H₆N₄O₄S₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 310.3

Ref: 10-F068526