AB72375
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $129.00 | $90.00 | - + | |
1g | 95% | in stock | $315.00 | $221.00 | - + | |
5g | 95% | in stock | $1,162.00 | $814.00 | - + | |
10g | 95% | in stock | $1,878.00 | $1,315.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB72375 |
Chemical Name: | Cyclohexylsulfamoyl chloride |
CAS Number: | 10314-35-9 |
Molecular Formula: | C6H12ClNO2S |
Molecular Weight: | 197.68298000000001 |
MDL Number: | MFCD11109158 |
SMILES: | ClS(=O)(=O)NC1CCCCC1 |
Complexity: | 203 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 1.9 |
N-Cyclohexylsulfamoyl chloride, also known as N-Cyclohexylsulfonyl chloride, is a versatile reagent used in chemical synthesis for a variety of applications. This compound is commonly employed as a sulfonylating agent, facilitating the introduction of the sulfamoyl functional group into organic molecules. In organic synthesis, N-Cyclohexylsulfamoyl chloride can serve as a key building block for the preparation of sulfonamides and related compounds. It reacts readily with nucleophiles such as amines, alcohols, and thiols to form sulfamoyl derivatives through nucleophilic substitution reactions. The resulting sulfamoyl-containing compounds exhibit diverse biological activities and are utilized in the development of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, N-Cyclohexylsulfamoyl chloride can be utilized in the synthesis of heterocyclic compounds, particularly in the preparation of sulfonamide heterocycles. These heterocyclic structures are of interest in medicinal chemistry due to their potential as bioactive molecules and drug candidates.Overall, N-Cyclohexylsulfamoyl chloride is a valuable reagent in chemical synthesis, enabling the efficient incorporation of sulfamoyl groups into organic molecules for the development of diverse compounds with potential applications in various fields.