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783-08-4

4-[5-(4-methylpiperazin-1-yl)-1h,1'h-2,5'-bibenzimidazol-2'-yl]benzenesulfonamide trihydrochloride

Catalog#: AR008NPF  |   CAS#: 783-08-4  |   MDL#: MFCD00025797  |   MF: C25H28Cl3N7O2S  |   MW: 596.9595

Packsize Purity Price Availability Quantity
100mg 95% $11.00 Global Stock Buy Now Add To Cart
250mg 95% $26.00 Global Stock Buy Now Add To Cart
1g 95% $77.00 Global Stock Buy Now Add To Cart
5g 95% $368.00 Global Stock Buy Now Add To Cart
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Catalog Number AR008NPF
Chemical Name 4-[5-(4-methylpiperazin-1-yl)-1h,1'h-2,5'-bibenzimidazol-2'-yl]benzenesulfonamide trihydrochloride
CAS Number 783-08-4
Molecular Formula C25H28Cl3N7O2S
Molecular Weight 596.9595
MDL Number MFCD00025797
SMILES CN1CCN(CC1)c1ccc2c(c1)nc([nH]2)c1ccc2c(c1)nc([nH]2)c1ccc(cc1)S(=O)(=O)N.Cl.Cl.Cl

The compound $name$ plays a crucial role in chemical synthesis as it serves as a key building block in the creation of novel pharmaceutical compounds and advanced materials. With its unique structure of 4-[5-(4-methylpiperazin-1-yl)-1H,1'H-2,5'-bibenzimidazol-2'-yl]benzenesulfonamide trihydrochloride, this compound offers a versatile platform for designing and synthesizing complex molecules with specific biological activities.In the realm of chemical synthesis, $name$ is utilized as a foundation for the development of potential drug candidates targeting various diseases. Its structural features allow for precise modifications and functionalization, enabling chemists to tailor its properties for enhanced drug potency, improved pharmacokinetics, and reduced toxicity. By incorporating $name$ into synthetic pathways, researchers can access a diverse array of pharmacophores and structural motifs, facilitating the discovery of new therapeutic agents.Moreover, $name$ exhibits remarkable reactivity and compatibility with a wide range of reaction conditions, making it a valuable reagent in organic chemistry. Its sulfonamide functionality can participate in key transformations such as amide bond formation, nucleophilic substitution, and metal-catalyzed cross-coupling reactions, enabling the construction of complex molecular architectures efficiently. This compound's trihydrochloride salt form enhances its solubility and stability, facilitating its manipulation in various experimental settings.Overall, the application of 4-[5-(4-methylpiperazin-1-yl)-1H,1'H-2,5'-bibenzimidazol-2'-yl]benzenesulfonamide trihydrochloride in chemical synthesis offers a promising avenue for the development of next-generation therapeutics and functional materials. Its versatility, reactivity, and structural diversity make it a valuable tool for advancing the frontiers of synthetic chemistry and drug discovery.
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