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Catalog Number:
37181
CAS Number:
96989-50-3
Di(2-pyridyl) thionocarbonate
Purity:
≥ 99.5% (Assay by titration)
Synonym(s):
O,O'-Di-2-pyridyl thiocarbonate, Thiocarbonic acid O,O'-Di-2-pyridyl ester
Documents
$20.00 /100MG
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Product Information

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.

Synonyms
O,O'-Di-2-pyridyl thiocarbonate, Thiocarbonic acid O,O'-Di-2-pyridyl ester
CAS Number
96989-50-3
Purity
≥ 99.5% (Assay by titration)
Molecular Formula
C11H8N2O2S
Molecular Weight
232.26
MDL Number
MFCD00074870
PubChem ID
719784
Melting Point
101 - 103 °C
Appearance
Pale cream powder
Conditions
Store at -20 °C
General Information
Synonyms
O,O'-Di-2-pyridyl thiocarbonate, Thiocarbonic acid O,O'-Di-2-pyridyl ester
CAS Number
96989-50-3
Purity
≥ 99.5% (Assay by titration)
Molecular Formula
C11H8N2O2S
Molecular Weight
232.26
MDL Number
MFCD00074870
PubChem ID
719784
Melting Point
101 - 103 °C
Appearance
Pale cream powder
Conditions
Store at -20 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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