Nombre del producto:tert-butyldimethyl{[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-3-en-1-yl]oxy}silane

IUPAC Name:tert-butyldimethyl{[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-3-en-1-yl]oxy}silane

CAS:251928-73-1
Fórmula molecular:C16H33BO3Si
Pureza:95%+
Número de catálogo:CM1047285
Peso molecular:312.33

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Detalles del producto

Núm. De CAS :251928-73-1
Fórmula molecular:C16H33BO3Si
Punto de fusión:-
Código de sonrisas:CC(C)(C)[Si](C)(C)OCCC(=C)B1OC(C)(C)C(C)(C)O1
Densidad:
Número de catálogo:CM1047285
Peso molecular:312.33
Punto de ebullición:
Nº Mdl:
Almacenamiento:

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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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ABBV-712
TYK2 is an attractive target for various autoimmune diseases as it regulates signal transduction downstream of IL-23 and IL-12 receptors. Selective TYK2 inhibition offers a differentiated clinical profile compared to currently approved JAK inhibitors. Scientists discovered the clinical candidate ABBV-712 in the optimization of selective TYK2 inhibitors targeting the pseudokinase domain.

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