CAS 83947-55-1
:trans-4,4,5,5-Tetramethyl-2-oct-1-enyl-1,3,2-dioxaborolane
Description:
Trans-4,4,5,5-Tetramethyl-2-oct-1-enyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane ring structure, which incorporates a boron atom and is typically used in organic synthesis, particularly in the formation of carbon-boron bonds. This compound features a trans configuration around the double bond, contributing to its stereochemical properties. The presence of multiple methyl groups enhances its steric bulk and can influence its reactivity and solubility in various solvents. Dioxaborolanes are known for their stability and ability to undergo hydrolysis, making them useful intermediates in synthetic chemistry. Additionally, this compound may exhibit specific optical properties due to its structural features, which can be relevant in applications such as materials science or pharmaceuticals. Its CAS number, 83947-55-1, allows for easy identification and reference in chemical databases. Overall, trans-4,4,5,5-Tetramethyl-2-oct-1-enyl-1,3,2-dioxaborolane is a versatile compound with significant implications in organic synthesis and related fields.
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
trans-1-Octenylboronic acid pinacol ester, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C14H27BO2Purity:97%Color and Shape:Clear colorless, LiquidMolecular weight:238.18Trans-1-Octenylboronic Acid Pinacol Ester
CAS:Formula:C14H27BO2Purity:98%Color and Shape:LiquidMolecular weight:238.1740trans-1-(Oct-1-en-1-yl)boronic acid, pinacol ester
CAS:trans-1-(Oct-1-en-1-yl)boronic acid, pinacol esterPurity:98%



