Product Name:Thiomorpholine-3-carbonitrile

IUPAC Name:thiomorpholine-3-carbonitrile

CAS:1206228-78-5
Molecular Formula:C5H8N2S
Purity:95%+
Catalog Number:CM388858
Molecular Weight:128.19

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Product Details

CAS NO:1206228-78-5
Molecular Formula:C5H8N2S
Melting Point:-
Smiles Code:N#CC1CSCCN1
Density:
Catalog Number:CM388858
Molecular Weight:128.19
Boiling Point:
MDL No:
Storage:

Product Other Information

Product Overview Thiomorpholine-3-carbonitrile, also known as TM3CN, is an organic compound that is used in a variety of scientific research applications. It is a versatile compound with a wide range of properties, making it an ideal choice for a variety of experiments.
Synthesis and Application Thiomorpholine-3-carbonitrile can be synthesized using a variety of methods, including the reaction of thiomorpholine-3-carboxylic acid with sodium cyanide in an aqueous solution. The reaction is carried out at room temperature and yields the desired compound in high yields. Other methods for synthesizing Thiomorpholine-3-carbonitrile include the reaction of thiomorpholine-3-carboxylic acid with thionyl chloride in a dichloromethane solution, as well as the reaction of thiomorpholine-3-carboxylic acid with sodium nitrite in an aqueous solution. Thiomorpholine-3-carbonitrile has a variety of scientific research applications, including its use as a reagent in organic synthesis, as a catalyst in the synthesis of heterocyclic compounds, as a ligand in coordination chemistry, as a reactant in the synthesis of polymers, and as a substrate in enzyme-catalyzed reactions. Thiomorpholine-3-carbonitrile is also used in the study of molecular recognition, molecular assembly, and molecular self-assembly.
Future Directions The future of Thiomorpholine-3-carbonitrile is promising, as it has a wide range of potential applications. These include its use as a reagent in organic synthesis, as a catalyst in the synthesis of heterocyclic compounds, as a ligand in coordination chemistry, as a reactant in the synthesis of polymers, and as a substrate in enzyme-catalyzed reactions. In addition, further research into its biochemical and physiological effects could lead to new therapeutic applications. Finally, its use in the study of molecular recognition, molecular assembly, and molecular self-assembly could lead to new insights into these areas.