Название продукции: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
Молекулярная формула:C16H33BO3Si
Чистота:95%+
Номер в каталоге:CM1047285
Молекулярная масса:312.33

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Информация о продукции

Номер CAS:251928-73-1
Молекулярная формула:C16H33BO3Si
Точка плавления:-
Smiles-код:CC(C)(C)[Si](C)(C)OCCC(=C)B1OC(C)(C)C(C)(C)O1
Плотность:
Номер в каталоге:CM1047285
Молекулярная масса:312.33
Точка кипения:
Номер Mdl:
Хранение:

Category 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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Column Infos

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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