Boronic acid, specifically the compound known as [1,1'-binaphthalen]-4-yl-, is characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a binaphthyl structure. This compound typically exhibits properties associated with both boronic acids and polycyclic aromatic hydrocarbons. It is likely to be a white to off-white solid, soluble in polar organic solvents, and may have limited solubility in water due to its hydrophobic binaphthyl backbone. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. Additionally, the compound may exhibit interesting optical properties due to the conjugated system of the naphthalene units, which can be leveraged in photonic applications. Its reactivity can be influenced by the presence of the boron atom, which can participate in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Overall, this compound represents a versatile building block in organic chemistry.

Boronic acid, [1,1'-binaphthalen]-4-yl-

363607-69-6: 1,1'-Binaphthyl-4-Ylboronicacid

[1,1'-Binaphthalen]-4-ylboronic acid

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CAS 363607-69-6: Boronic acid, [1,1'-binaphthalen]-4-yl-

[1,1'-Binaphthalen]-4-ylboronic acid

Ref: 54-OR360112

[1,1'-Binaphthalen]-4-ylboronic acid

Ref: 3D-FB143751

[1,1'-Binaphthalen]-4-ylboronic acid

Ref: 10-F213072

[1,1'-Binaphthalen]-4-ylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-N1010

[1,1'-Binaphthalen]-4-ylboronic acid

Ref: IN-DA007A3X