AB76966
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
5g | 95% | in stock | $25.00 | $17.00 | - + | |
25g | 95% | in stock | $25.00 | $18.00 | - + | |
100g | 95% | in stock | $73.00 | $51.00 | - + | |
500g | 95% | in stock | $249.00 | $175.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB76966 |
Chemical Name: | N-Acetylsulfanilyl chloride |
CAS Number: | 121-60-8 |
Molecular Formula: | C8H8ClNO3S |
Molecular Weight: | 233.67202000000006 |
MDL Number: | MFCD00007442 |
SMILES: | CC(=O)Nc1ccc(cc1)S(=O)(=O)Cl |
NSC Number: | 127860 |
Complexity: | 301 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 1.4 |
$Name$ is a versatile compound commonly used in chemical synthesis for its reactivity and functionality. In particular, 4-Acetamidobenzene-1-sulfonyl chloride serves as a valuable reagent in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its sulfonyl chloride group can selectively react with nucleophiles to introduce the sulfonyl functionality into target molecules, enabling the formation of sulfonamides, sulfonylureas, and other sulfonylated compounds. This reagent is known for its robustness and efficiency in chemical transformations, making it a preferred choice in organic synthesis for the modification and derivatization of complex molecules.
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