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CAS 5122-99-6

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4-Iodophenylboronic acid

Description:
4-Iodophenylboronic acid is an organoboron compound characterized by the presence of both a boronic acid group and an iodine atom attached to a phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl group that is further substituted with an iodine atom at the para position. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile building block for the formation of biaryl compounds. The presence of the iodine atom enhances its reactivity and facilitates various transformations. Additionally, 4-iodophenylboronic acid can act as a ligand in coordination chemistry and has potential applications in medicinal chemistry due to its ability to interact with biological targets. Safety precautions should be observed when handling this compound, as boronic acids can be irritants and the iodine moiety may pose additional hazards.
Formula:C6H6BIO2
InChI:InChI=1/C6H6BIO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI key:PELJYVULHLKXFF-UHFFFAOYSA-N
SMILES:c1cc(ccc1B(O)O)I
Synonyms:
  • p-Iodobenzeneboronic acid
  • Benzeneboronic acid, p-iodo-
  • P-Iodophenylboronic Acid
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