Boronic acid, specifically (3,3,3-trifluoropropyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a hydroxyl group and a trifluoropropyl group. Its molecular structure features a three-carbon chain with three fluorine atoms attached to the terminal carbon, which significantly influences its chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and materials science, particularly in the development of sensors and drug delivery systems. The trifluoropropyl group enhances the compound's lipophilicity and stability, which can affect its reactivity and interactions in various chemical environments. Additionally, boronic acids can participate in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds in organic chemistry. Overall, (3,3,3-trifluoropropyl)boronic acid is a versatile compound with applications in synthetic organic chemistry and materials development.

Boronic acid, (3,3,3-trifluoropropyl)-

674-55-5: Boronic acid, specifically (3,3,3-trifluoropropyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a hydroxyl group and a trifluoropropyl group. Its molecular structure features a three-carbon chain with three fluorine atoms attached to the terminal carbon, which significantly influences its chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and materials science, particularly in the development of sensors and drug delivery systems. The trifluoropropyl group enhances the compound's lipophilicity and stability, which can affect its reactivity and interactions in various chemical environments. Additionally, boronic acids can participate in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds in organic chemistry. Overall, (3,3,3-trifluoropropyl)boronic acid is a versatile compound with applications in synthetic organic chemistry and materials development.

CAS 674-55-5

Boronic acid, (3,3,3-trifluoropropyl)-

(3,3,3-Trifluoropropyl)boronic acid

Ref: IN-DA0039KC

(3,3,3-Trifluoropropyl)boronic acid

Ref: 10-F720201