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CAS 57404-76-9

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(1E)-hept-1-en-1-ylboronic acid

Description:
(1E)-hept-1-en-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a terminal alkene. It features a seven-carbon chain with a double bond at the first carbon, which contributes to its reactivity and potential applications in organic synthesis. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical reactions, including Suzuki coupling, which is widely used in the formation of carbon-carbon bonds. This compound is typically a colorless to pale yellow liquid and is soluble in polar organic solvents. Its reactivity is influenced by the presence of both the alkene and the boronic acid moiety, allowing it to participate in diverse chemical transformations. Additionally, (1E)-hept-1-en-1-ylboronic acid can serve as a building block in the synthesis of more complex molecules, particularly in medicinal chemistry and materials science. Safety precautions should be taken when handling this compound, as with all organoboron compounds, due to potential reactivity and toxicity.
Formula:C7H15BO2
InChI:InChI=1/C7H15BO2/c1-2-3-4-5-6-7-8(9)10/h6-7,9-10H,2-5H2,1H3/b7-6+
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90
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