CAS 873566-75-7

(3-amino-4-fluorophenyl)boronic acid

Description:

(3-Amino-4-fluorophenyl)boronic acid is an organic compound characterized by the presence of both an amino group and a boronic acid functional group attached to a phenyl ring. The molecular structure features a fluorine atom at the para position relative to the amino group, which can influence its reactivity and solubility. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group. It is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to form reversible covalent bonds with diols. The boronic acid moiety also plays a crucial role in cross-coupling reactions, such as Suzuki-Miyaura coupling, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the amino and fluorine substituents can enhance its biological activity and selectivity in various applications.

Formula: C₆H₇BFNO₂

InChI: InChI=1/C6H7BFNO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,10-11H,9H2

SMILES: c1cc(c(cc1B(O)O)N)F

Synonyms:

• boronic acid, B-(3-amino-4-fluorophenyl)-
• 3-Amino-4-fluorophenylboronicacid
• 3-Amino-4-fluorophenylboronic acid, pinacol ester

3-Amino-4-fluorophenylboronic acid

CAS: 873566-75-7

Formula: C₆H₇BFNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 154.9347

Ref: IN-DA0036D2

3-Amino-4-fluorobenzeneboronic acid

CAS: 873566-75-7

3-Amino-4-fluorobenzeneboronic acid

Formula: C₆H₇BFNO₂

Purity: 97%

Color and Shape: Off-White Powder

Molecular weight: 154.93g/mol

Ref: 54-PC3218

3-Amino-4-fluorophenylboronic acid

CAS: 873566-75-7

Formula: C₆H₇BFNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 154.94

Ref: 10-F221725