CAS 42599-16-6
:E-Octen-1-ylboronic acid
Description:
E-Octen-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to an octene chain. This compound typically features a double bond in the octene portion, which is in the E (trans) configuration, indicating that the substituents on either end of the double bond are on opposite sides. E-Octen-1-ylboronic acid is known for its reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The boronic acid group allows for the formation of stable complexes with diols and is useful in various applications, including the development of sensors and drug delivery systems. Additionally, this compound may exhibit moderate solubility in organic solvents and can participate in various chemical transformations, such as Suzuki-Miyaura coupling, which is a key reaction in the formation of carbon-carbon bonds. Its properties make it a significant building block in the synthesis of more complex organic molecules.
Formula:C8H17BO2
InChI:InChI=1/C8H17BO2/c1-2-3-4-5-6-7-8-9(10)11/h7-8,10-11H,2-6H2,1H3/b8-7+
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