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Catalog Number:
37181
CAS Number:
96989-50-3
Di(2-pyridyl)thionocarbonate
Purity:
≥ 99,5 % (dosage par titration)
Synonym(s):
Thiocarbonate de O,O'-Di-2-pyridyle, Ester d'acide thiocarbonique O , O' -Di-2-pyridyle
Documents
$20.00 /100 mg
Taille
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Informations sur le produit

Di(2-pyridyl) thionocarbonate is a versatile compound known for its unique properties and applications in various fields, particularly in organic synthesis and materials science. This compound, also recognized as dipyridin-2-yloxymethanethione, serves as an effective reagent in the preparation of thioesters and thioamides, making it invaluable for researchers engaged in synthetic chemistry. Its ability to facilitate the formation of carbon-sulfur bonds enhances its utility in the development of pharmaceuticals, agrochemicals, and specialty chemicals.

Moreover, Di(2-pyridyl) thionocarbonate exhibits excellent stability and reactivity, which allows for its use in diverse chemical transformations. It is particularly beneficial in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development. Researchers appreciate its efficiency in reactions, leading to higher yields and reduced reaction times compared to similar compounds. This compound not only streamlines synthetic pathways but also opens avenues for innovative applications in advanced materials and nanotechnology.

Numéro CAS 
96989-50-3
Formule moléculaire
C11H8N2O2S
Poids moléculaire 
232.26
Point de fusion 
101 - 103 °C
Informations générales
Numéro CAS 
96989-50-3
Formule moléculaire
C11H8N2O2S
Poids moléculaire 
232.26
Point de fusion 
101 - 103 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Di(2-pyridyl) thionocarbonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the formation of various sulfur-containing compounds, which are essential in creating pharmaceuticals and agrochemicals.
  • Coordination Chemistry: It acts as a ligand in coordination complexes, enhancing the properties of metal ions. This application is particularly valuable in catalysis and materials science.
  • Biological Studies: Researchers use it to explore biochemical pathways, as it can interact with biological molecules, aiding in the development of new drugs or understanding disease mechanisms.
  • Polymer Chemistry: The compound is employed in the synthesis of polymers, providing unique properties such as increased thermal stability and enhanced mechanical strength, which are crucial for advanced materials.
  • Analytical Chemistry: It is utilized in various analytical techniques, including spectroscopy, to detect and quantify sulfur compounds in environmental samples, ensuring compliance with safety regulations.

Citations