Product Description:
2-(2-Bromobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boronic ester used in organic synthesis and is known for its reactivity in Suzuki coupling reactions.
Applications & Uses:
CAS#:
153020-83-0
SYNONYM:
2-(2-Bromobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-Bromobenzylboronic acid pinacol ester
FORMULA:
C13H18BBrO2
PRODUCT TYPE:
HAZARD:
Warning
CATEGORIES:
Organic Intermediate
,
Alkyl Bromides
,
Aromatic Bromides
,
Specialty Chemicals
Technical Specifications
Appearance :
white to off-white solid
Boiling Point, °C :
128-130
Density, g/cm3 :
1.22
Flash Point, °C :
128
Melting point, °C :
36-39
Molecular weight, g/mol :
295.96
Purity, % :
98
Refractive index, n20/D :
1.522
2-(2-Bromobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a specialized organoboron compound used primarily in the field of organic synthesis. Its bromobenzyl group, combined with the stable dioxaborolane ring structure, makes it a valuable reagent for Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds with precision and efficiency. This compound is ideal for chemists seeking to create complex molecules in the pharmaceutical and agrochemical industries, owing to its ability to participate in palladium-catalyzed procedures. With its distinctive molecular structure, it serves as a versatile building block in the synthesis of various biologically active compounds and fine chemicals, offering reliability and consistency in demanding synthetic pathways.