cas 1233526-31-2|| where to buy 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)tetrahydrothiophene 1,1-dioxide

Nombre del producto:3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)tetrahydrothiophene 1,1-dioxide

IUPAC Name:3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]-1λ⁶-thiolane-1,1-dione

: CAS：1233526-31-2; Fórmula molecular：C13H21BN2O4S; Pureza：95%+

: Número de catálogo：CM135932; Peso molecular：312.19

Unidad de embalaje	Stock disponible	Precio($)	Cantidad
CM135932-10g	in stock	Ɠƥůƥ

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Detalles del producto

: Núm. De CAS :1233526-31-2; Fórmula molecular:C13H21BN2O4S; Punto de fusión:-; Código de sonrisas:CC1(C)C(C)(C)OB(C2=CN(C(CC3)CS3(=O)=O)N=C2)O1; Densidad:

: Número de catálogo:CM135932; Peso molecular:312.19; Punto de ebullición:; Nº Mdl:MFCD18383245; Almacenamiento:

Category Infos

: Pyrazoles; Pyrazoles are organic compounds of the general formula C3H3N2H. It is a five-membered heterocycle consisting of three carbon atoms and two adjacent nitrogen atoms. As an H-bond-donating heterocycle, pyrazole has been used as a more lipophilic and metabolically more stable bioisomer of phenol. Pyrazoles have attracted more and more attention due to their broad spectrum of action and strong efficacy.; Pyrazone; Custom pyrazone for customers from all over the world are our main business.

: Tetrahydrothiophenes; Tetrahydrothiophene is a sulfur-containing saturated heterocyclic compound obtained by catalytic hydrogenation of thiophene. After thiophene is reduced to tetrahydrothiophene, it no longer has a conjugated system and aromaticity. Therefore, tetrahydrothiophene shows the properties of general thioethers. Easily oxidized to sulfoxides and sulfones. Tetrahydrothiophene can be used as a raw material for the production of pharmaceuticals, pesticides and photochemicals.

Column Infos

: Boronic Acids and Esters; Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).

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