Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The specific compound "Boronic acid, B-[4-(1-methylethoxy)phenyl]-, hydrate (1:1)" features a boron atom attached to a phenyl group that has a 1-methylethoxy substituent, which contributes to its hydrophobic properties. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. The hydrate form indicates that the compound can associate with water molecules, which may influence its solubility and reactivity. Boronic acids generally exhibit Lewis acidity, allowing them to interact with various nucleophiles. Additionally, they can form stable complexes with diols, making them useful in sensor applications and drug delivery systems. The presence of the methylethoxy group enhances its steric properties, potentially affecting its reactivity and interaction with biological systems. Overall, this compound is significant in both synthetic organic chemistry and materials science.

Boronic acid, B-[4-(1-methylethoxy)phenyl]-, hydrate (1:1)

1256355-64-2: Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The specific compound "Boronic acid, B-[4-(1-methylethoxy)phenyl]-, hydrate (1:1)" features a boron atom attached to a phenyl group that has a 1-methylethoxy substituent, which contributes to its hydrophobic properties. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. The hydrate form indicates that the compound can associate with water molecules, which may influence its solubility and reactivity. Boronic acids generally exhibit Lewis acidity, allowing them to interact with various nucleophiles. Additionally, they can form stable complexes with diols, making them useful in sensor applications and drug delivery systems. The presence of the methylethoxy group enhances its steric properties, potentially affecting its reactivity and interaction with biological systems. Overall, this compound is significant in both synthetic organic chemistry and materials science.

CAS 1256355-64-2

Boronic acid, B-[4-(1-methylethoxy)phenyl]-, hydrate (1:1)

4-Isopropoxyphenylboronic acid, hydrate

Ref: IN-DA000O59

4-Isopropoxyphenylboronic acid,hydrate

Ref: 54-OR360542