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52480-31-6

6-chloro-N,N-dimethylpyridine-3-sulfonamide

Catalog#: AR019WL1  |   CAS#: 52480-31-6  |   MDL#: MFCD01928039  |   MF: C7H9ClN2O2S  |   MW: 220.67656

Packsize Purity Price Availability Quantity
50mg 95% $164.00 2-3 weeks Buy Now Add To Cart
100mg 95% $234.00 2-3 weeks Buy Now Add To Cart
250mg 95% $322.00 2-3 weeks Buy Now Add To Cart
500mg 95% $585.00 2-3 weeks Buy Now Add To Cart
1g 95% $751.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,447.00 2-3 weeks Buy Now Add To Cart
5g 95% $2,129.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR019WL1
Chemical Name 6-chloro-N,N-dimethylpyridine-3-sulfonamide
CAS Number 52480-31-6
Molecular Formula C7H9ClN2O2S
Molecular Weight 220.67656
MDL Number MFCD01928039
SMILES Clc1ccc(cn1)S(=O)(=O)N(C)C

6-chloro-N,N-dimethylpyridine-3-sulfonamide, also known as $name$, is a versatile compound widely used in chemical synthesis as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It serves as a valuable building block for the synthesis of heterocyclic compounds, particularly in the development of new drug molecules.In chemical synthesis, $name$ plays a crucial role in the formation of complex organic structures through its reactivity and functional group compatibility. Its sulfonamide moiety provides a handle for introducing other functional groups, enabling the creation of diverse chemical entities with specific properties and activities.One of the important applications of 6-chloro-N,N-dimethylpyridine-3-sulfonamide is in the synthesis of sulfa drugs, a class of antibiotics that inhibit bacterial growth by targeting essential metabolic pathways. By incorporating this compound into the molecular scaffold of sulfa drugs, researchers can tailor their pharmacokinetic properties and enhance their therapeutic efficacy.Furthermore, the presence of a chloro substituent on the pyridine ring enhances the nucleophilicity and electrophilicity of $name$, making it a valuable reagent for various organic transformations. It can participate in nucleophilic substitution, addition reactions, and metal-catalyzed coupling reactions, enabling the synthesis of structurally diverse compounds with high efficiency and selectivity.Overall, 6-chloro-N,N-dimethylpyridine-3-sulfonamide serves as a versatile and indispensable tool in modern chemical synthesis, facilitating the development of new molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.
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