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CAS 215951-86-3

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[(1E)-3-chloroprop-1-en-1-yl]boronic acid

Description:
[(1E)-3-chloroprop-1-en-1-yl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a vinyl chloride moiety. This compound features a boron atom bonded to a hydroxyl group and an alkene, specifically a propene derivative with a chlorine substituent. The presence of the boronic acid group imparts unique reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in polar organic solvents, which facilitates its use in various chemical reactions. The chloropropenyl group enhances its electrophilic character, allowing it to participate in nucleophilic attacks. Safety considerations include handling it with care due to potential toxicity and reactivity, particularly in the presence of moisture, which can lead to hydrolysis of the boronic acid group. Overall, [(1E)-3-chloroprop-1-en-1-yl]boronic acid is a versatile intermediate in the synthesis of more complex organic molecules.
Formula:C3H6BClO2
InChI:InChI=1/C3H6BClO2/c5-3-1-2-4(6)7/h1-2,6-7H,3H2/b2-1+
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