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56236-82-9

4-cyano-N-methylbenzene-1-sulfonamide

Catalog#: AR019NNJ  |   CAS#: 56236-82-9  |   MDL#: MFCD08869212  |   MF: C8H8N2O2S  |   MW: 196.2263

Packsize Purity Price Availability Quantity
100mg 95% $71.00 Global Stock Buy Now Add To Cart
250mg 95% $120.00 Global Stock Buy Now Add To Cart
1g 95% $324.00 Global Stock Buy Now Add To Cart
5g 95% $1,132.00 Global Stock Buy Now Add To Cart
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Catalog Number AR019NNJ
Chemical Name 4-cyano-N-methylbenzene-1-sulfonamide
CAS Number 56236-82-9
Molecular Formula C8H8N2O2S
Molecular Weight 196.2263
MDL Number MFCD08869212
SMILES CNS(=O)(=O)c1ccc(cc1)C#N

4-Cyano-N-methylbenzenesulfonamide, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound is commonly employed as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and reactivity make it a key intermediate in the synthesis of diverse organic compounds.One of the main applications of 4-Cyano-N-methylbenzenesulfonamide is in the formation of sulfonamide derivatives. By reacting with various nucleophiles or electrophiles, this compound can undergo substitution, addition, or condensation reactions to form structurally complex molecules with specific functionalities. These sulfonamide derivatives often exhibit enhanced biological activities, making them important in medicinal chemistry for developing new drugs.Moreover, 4-Cyano-N-methylbenzenesulfonamide can serve as a precursor for the synthesis of heterocyclic compounds. Through cyclization reactions, this compound enables the construction of nitrogen-containing rings, which are prevalent in many biologically active molecules and natural products. This versatility in forming diverse chemical structures highlights the significance of 4-Cyano-N-methylbenzenesulfonamide in organic synthesis.Additionally, the presence of the cyano group in this compound enhances its utility as a synthetic intermediate. The cyano group can undergo various transformations, such as reduction, hydrolysis, or cyanation, leading to the preparation of compounds with different chemical properties and functionalities. This flexibility in modifying the cyano group expands the synthetic applications of 4-Cyano-N-methylbenzenesulfonamide in developing novel compounds for pharmaceutical, agricultural, and material science purposes.
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