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96989-50-3

O,O-Di(pyridin-2-yl) carbonothioate

Catalog#: AR0035E5  |   CAS#: 96989-50-3  |   MDL#: MFCD00074870  |   MF: C11H8N2O2S  |   MW: 232.2584

Packsize Purity Price Availability Quantity
100mg 97% $5.00 Global Stock Buy Now Add To Cart
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $7.00 Global Stock Buy Now Add To Cart
5g 97% $25.00 Global Stock Buy Now Add To Cart
25g 97% $90.00 Global Stock Buy Now Add To Cart
100g 97% $297.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0035E5
Chemical Name O,O-Di(pyridin-2-yl) carbonothioate
CAS Number 96989-50-3
Molecular Formula C11H8N2O2S
Molecular Weight 232.2584
MDL Number MFCD00074870
SMILES S=C(Oc1ccccn1)Oc1ccccn1

O,O-Di(pyridin-2-yl) carbonothioate is a versatile compound widely utilized in chemical synthesis for its unique properties and applications. This compound is commonly employed as a reactive intermediate in organic reactions due to its ability to act as a donor of different functional groups, such as carbonothioate and pyridinyl moieties.One of the key applications of O,O-Di(pyridin-2-yl) carbonothioate is in the synthesis of heterocyclic compounds. Its sulfur-containing carbonothioate group provides a reactive site for nucleophilic substitutions, enabling the efficient formation of various sulfur-containing heterocycles. These heterocyclic compounds play a crucial role in the pharmaceutical industry as they often exhibit diverse biological activities.Furthermore, O,O-Di(pyridin-2-yl) carbonothioate can also be utilized in transition metal-catalyzed cross-coupling reactions. The pyridinyl groups attached to the carbonothioate moiety can facilitate coordination with transition metal catalysts, enabling efficient C-C bond formation. This property makes it a valuable building block for the synthesis of complex organic molecules with diverse chemical functionalities.In summary, O,O-Di(pyridin-2-yl) carbonothioate is a versatile compound that finds wide-ranging applications in chemical synthesis, particularly in the construction of heterocyclic compounds and in transition metal-catalyzed reactions. Its unique reactivity and functional groups make it an indispensable tool for organic chemists seeking to access structurally diverse and complex molecules.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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