CAS 159087-42-0
:1,3,2-Dioxaborolane, 2-(5-chloro-1-pentynyl)-4,4,5,5-tetramethyl-
Description:
1,3,2-Dioxaborolane, 2-(5-chloro-1-pentynyl)-4,4,5,5-tetramethyl- is an organoboron compound characterized by its dioxaborolane ring structure, which features a five-membered cyclic arrangement containing two oxygen atoms and a boron atom. This compound is notable for its functionalization with a 5-chloro-1-pentynyl group, contributing to its reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The presence of tetramethyl substituents enhances its steric bulk, which can influence its reactivity and solubility in various solvents. Typically, compounds of this nature are utilized in the development of pharmaceuticals, agrochemicals, and materials science due to their unique chemical properties. Additionally, the chlorine atom in the alkynyl group may serve as a leaving group or participate in further chemical transformations. Overall, this compound exemplifies the versatility of boron-containing compounds in synthetic organic chemistry.
Formula:C11H18BClO2
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
1,3,2-Dioxaborolane, 2-(5-chloro-1-pentyn-1-yl)-4,4,5,5-tetramethyl-
CAS:Formula:C11H18BClO2Purity:95%Molecular weight:228.52345-Chloropent-1-ynylboronic acid, pinacol ester
CAS:5-Chloropent-1-ynylboronic acid, pinacol esterPurity:≥95%Molecular weight:228.52g/mol2-(5-Chloropent-1-yn-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C11H18BClO2Purity:95.0%Color and Shape:LiquidMolecular weight:228.52


