4-Nonylphenylboronic acid

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4-Nonylphenylboronic acid is a type of boronic acid that is commonly used in organic chemistry. It is a white, crystalline solid that is soluble in water and most organic solvents.

Chemical Structure[edit | edit source]

The chemical structure of 4-Nonylphenylboronic acid consists of a phenyl group attached to a boron atom, which is also attached to a nonyl group. The boron atom is also attached to two hydroxyl groups, which gives the compound its acidic properties.

Synthesis[edit | edit source]

4-Nonylphenylboronic acid can be synthesized through a Suzuki reaction, which involves the coupling of a boronic acid with a halide in the presence of a palladium catalyst. The nonyl group can be introduced through a Grignard reaction with nonyl bromide.

Applications[edit | edit source]

4-Nonylphenylboronic acid is primarily used in the synthesis of other organic compounds. It is a versatile reagent in cross-coupling reactions, particularly in the Suzuki reaction. It can also be used in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals.

Safety[edit | edit source]

Like all boronic acids, 4-Nonylphenylboronic acid should be handled with care. It can cause skin and eye irritation, and may be harmful if swallowed or inhaled. Appropriate safety measures should be taken when handling this compound.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD