cas 1353951-75-3|| where to buy (1-((2,4-dichlorophenyl)sulfonyl)piperidin-4-yl)methanol

Nombre del producto:(1-((2,4-dichlorophenyl)sulfonyl)piperidin-4-yl)methanol

IUPAC Name:[1-(2,4-dichlorobenzenesulfonyl)piperidin-4-yl]methanol

: CAS：1353951-75-3; Fórmula molecular：C12H15Cl2NO3S; Pureza：95%+

Unidad de embalaje	Stock disponible	Precio($)
CM179942-100mg	in stock	ǕǕƻ
CM179942-250mg	in stock	ǕǺș
CM179942-1g	in stock	ŭňǕ

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: Núm. De CAS :1353951-75-3; Fórmula molecular:C12H15Cl2NO3S; Punto de fusión:-; Código de sonrisas:OCC1CCN(S(=O)(C2=CC=C(Cl)C=C2Cl)=O)CC1; Densidad:

: Número de catálogo:CM179942; Peso molecular:324.22; Punto de ebullición:; Nº Mdl:MFCD21098950; Almacenamiento:

: Piperidines; Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.; Piperidine,Piperidine Price; if you want to know the latest news about piperidine and piperidine price, please come to our website and get a quote for free.

Product Overview	(1-((2,4-Dichlorophenyl)sulfonyl)piperidin-4-yl)methanol is a chemical compound that has been studied for its potential applications in scientific research.
Physical Properties	It is low solubility in aqueous solutions, which can make it difficult to use in certain experiments.
Synthesis Method	The synthesis of (1-((2,4-Dichlorophenyl)sulfonyl)piperidin-4-yl)methanol involves the reaction of 2,4-dichlorobenzenesulfonyl chloride with piperidin-4-ol in the presence of a base.
Synthesis and Application	It has been found to be a potent inhibitor of protein kinase CK2, which is involved in various cellular processes, such as cell proliferation and differentiation. This compound has also been studied for its potential anticancer activity, as CK2 is overexpressed in many cancer cells.
Future Directions	One area of research is the development of more soluble analogs of this compound, which would make it easier to use in various experiments. Another area of research is the exploration of the potential anticancer activity of this compound, as CK2 is overexpressed in many cancer cells. Additionally, the role of CK2 in various cellular processes, such as cell proliferation and differentiation, could be further studied using this compound.