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58804-19-6

4-(chloromethyl)-N,N-dimethylbenzene-1-sulfonamide

Catalog#: AR01A46Q  |   CAS#: 58804-19-6  |   MDL#: MFCD19321817  |   MF: C9H12ClNO2S  |   MW: 233.7151

Packsize Purity Price Availability Quantity
50mg 95% $281.00 2-3 weeks Buy Now Add To Cart
100mg 95% $406.00 2-3 weeks Buy Now Add To Cart
250mg 95% $570.00 2-3 weeks Buy Now Add To Cart
500mg 95% $883.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,125.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01A46Q
Chemical Name 4-(chloromethyl)-N,N-dimethylbenzene-1-sulfonamide
CAS Number 58804-19-6
Molecular Formula C9H12ClNO2S
Molecular Weight 233.7151
MDL Number MFCD19321817
SMILES ClCc1ccc(cc1)S(=O)(=O)N(C)C

4-(Chloromethyl)-N,N-dimethylbenzenesulfonamide is a versatile compound used in chemical synthesis for its unique reactivity and selectivity. This compound is commonly employed as a sulfonamide protecting group in organic synthesis reactions. Its ability to form stable sulfonamide linkages allows for the protection of various functional groups during complex chemical transformations.Additionally, 4-(Chloromethyl)-N,N-dimethylbenzenesulfonamide serves as a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its chloromethyl group provides a handle for further functionalization through nucleophilic substitution reactions, enabling the introduction of diverse substituents that influence the compound's activity and properties.Furthermore, this compound can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form biaryl compounds with high efficiency. Its dimethylbenzenesulfonamide moiety offers a unique steric and electronic environment that can influence the regioselectivity and yield of the coupling reactions.In conclusion, the application of 4-(Chloromethyl)-N,N-dimethylbenzenesulfonamide in chemical synthesis extends beyond simple protection strategies, making it a valuable tool for the construction of complex organic molecules with tailored properties and functions.
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