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Catalog Number:
14354
CAS Number:
2127-10-8
2,2'-Dithio-bis(5-nitropyridine)
Purity:
≥ 98% (HPLC)
Synonym(s):
Bis(5-Nitro-2-pyridyl) disulfide
Documents
$113.70 /1G
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Product Information

2,2'-Dithio-bis(5-nitropyridine) is a versatile compound recognized for its unique disulfide structure, which enhances its reactivity and potential applications in various fields. This compound is particularly valuable in organic synthesis and materials science, where it serves as a key intermediate in the development of novel pharmaceuticals and agrochemicals. Its ability to form stable complexes with metals makes it an excellent candidate for catalysis and coordination chemistry, facilitating reactions that are essential in the production of fine chemicals and specialty materials.

Researchers have also explored its utility in the field of electrochemistry, where it can be employed in the design of sensors and energy storage devices. The presence of nitro groups in its structure contributes to its electron-withdrawing properties, making it suitable for applications that require enhanced electronic characteristics. With its diverse applications and unique properties, 2,2'-Dithio-bis(5-nitropyridine) stands out as a valuable compound for professionals seeking innovative solutions in chemical research and industrial applications.

Synonyms
Bis(5-Nitro-2-pyridyl) disulfide
CAS Number
2127-10-8
Purity
≥ 98% (HPLC)
Molecular Formula
C10H6N4O4S2
Molecular Weight
310.3
MDL Number
MFCD00006453
PubChem ID
16474
Melting Point
142 - 149 ºC
Appearance
Yellow or tan solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Bis(5-Nitro-2-pyridyl) disulfide
CAS Number
2127-10-8
Purity
≥ 98% (HPLC)
Molecular Formula
C10H6N4O4S2
Molecular Weight
310.3
MDL Number
MFCD00006453
PubChem ID
16474
Melting Point
142 - 149 ºC
Appearance
Yellow or tan solid
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,2'-Dithio-bis(5-nitropyridine) is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the formation of disulfide bonds, which are crucial in the synthesis of various organic molecules.
  • Pharmaceutical Development: It is employed in the design of new drugs, particularly in creating compounds with enhanced biological activity due to its unique structural properties.
  • Material Science: The compound is used in developing advanced materials, such as polymers and coatings, that require specific chemical properties, including stability and resistance to degradation.
  • Analytical Chemistry: It acts as a reagent in analytical techniques, helping to detect and quantify other chemical substances, which is essential in quality control processes.
  • Biochemical Research: Researchers utilize it to study biological systems, particularly in exploring the role of disulfide bonds in protein structure and function, contributing to advancements in biochemistry.

Citations