CAS 881913-20-8

3-(1-Naphthyl)phenylboronic acid

Description:

3-(1-Naphthyl)phenylboronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and aromatic rings. It features a boron atom bonded to a hydroxyl group and two aromatic moieties: a phenyl group and a naphthyl group. This compound is typically used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds. The presence of the boronic acid group allows for the formation of stable complexes with diols and sugars, making it useful in biochemical applications as well. Its solubility is generally influenced by the nature of the substituents on the aromatic rings, and it may exhibit moderate solubility in polar organic solvents. Additionally, 3-(1-Naphthyl)phenylboronic acid can participate in various chemical reactions, including nucleophilic substitutions and coordination chemistry, making it a versatile building block in the synthesis of more complex organic molecules. Safety data should be consulted for handling and storage, as with all chemical substances.

Synonyms:

• 3-(Naphthalen-1-yl)phenylboronic acid
• Boronic acid, [3-(1-naphthalenyl)phenyl]-

BORONIC ACID, [3-(1-NAPHTHALENYL)PHENYL]-

CAS: 881913-20-8

Formula: C₁₆H₁₃BO₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 248.0842

Ref: IN-DA008BJ4

3-(1-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)

CAS: 881913-20-8

Formula: C₁₆H₁₃BO₂

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 248.09

Ref: 3B-N1131

[3-(1-Naphthyl)phenyl]boronic acid

CAS: 881913-20-8

[3-(1-Naphthyl)phenyl]boronic acid

Purity: 98%

Molecular weight: 248.08g/mol

Ref: 54-OR361692

(3-(Naphthalen-1-yl)phenyl)boronic acid

CAS: 881913-20-8

Formula: C₁₆H₁₃BO₂

Purity: 98%

Color and Shape: Liquid, No data available.

Molecular weight: 248.09

Ref: 10-F223857