CAS 25487-66-5

3-Carboxybenzeneboronic acid

Description:

3-Carboxybenzeneboronic acid, with the CAS number 25487-66-5, is an organic compound that features both a carboxylic acid and a boronic acid functional group. This compound is characterized by its aromatic ring, which is substituted with a carboxyl group (-COOH) and a boronic acid group (-B(OH)2) at the meta position. The presence of these functional groups imparts unique properties, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound is typically a white to off-white solid and is soluble in polar solvents like water and alcohols. Its reactivity is influenced by the boron atom, which can participate in coordination chemistry and catalysis. Additionally, 3-carboxybenzeneboronic acid can serve as a building block in the synthesis of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with biomolecules also makes it of interest in biochemical research.

Formula: C₇H₇BO₄

InChI: InChI=1/C7H7BO4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,11-12H,(H,9,10)

InChI key: InChIKey=DBVFWZMQJQMJCB-UHFFFAOYSA-N

SMILES: B(O)(O)C1=CC(C(O)=O)=CC=C1

Synonyms:

• 3-(Dihydroxyborane)benzoic acid
• 3-(Dihydroxyboranyl)benzoic acid
• 3-(Dihydroxyboryl)benzoic acid
• 3-Boronobenzoic Acid
• 3-Carboxyphenylboronic acid
• Benzoic acid, 3-borono-
• Benzoic acid, m-borono-
• M-Carboxybenzeneboronicacid
• [3-(Formyloxy)phenyl]boronic acid
• boronic acid, B-[3-(formyloxy)phenyl]-
• m-Carboxyphenylboronic acid
• 3-Carboxybenzeneboronic acid
• 3-Carboxypenylboronic Acid
• 3-(DIHYDROXYBORONYL)BENZOIC ACID
• (3-Formyloxyphenyl)boronicacid
• AKOS BRN-0007
• RARECHEM AH PB 0148
• 3-Carboxyphenylboronic acid, min. 97%
• 3-Carboxyphenylboronicacid,min.97%
• m-borono-benzoicaci
• 3-CARBOXYBENZENEBORONIC ACID 98%
• 3-Carboxyphenylboronic acid ,98%
• 3-borono-benzoicaci
• 3-Carboxyphenylboronic Acid (contains varying amounts of Anhydride)

3-Carboxyphenylboronic Acid (contains varying amounts of Anhydride)

CAS: 25487-66-5

Formula: C₇H₇BO₄

Purity: 97.0 to 112.0 %

Color and Shape: White to Orange to Green powder to crystal

Molecular weight: 165.94

Ref: 3B-C2028

3-Boronobenzoic acid

CAS: 25487-66-5

Formula: C₇H₇BO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 165.9391

Ref: IN-DA003J5Y

3-Carboxyphenylboronic acid

CAS: 25487-66-5

Formula: C₇H₇BO₄

Molecular weight: 165.94

Ref: 7W-GK2099

3-Carboxybenzeneboronic acid

CAS: 25487-66-5

3-Carboxybenzeneboronic acid

Formula: C₇H₇BO₄

Purity: ≥95%

Color and Shape: white to off-white solid

Molecular weight: 165.94g/mol

Ref: 54-OR4442

Benzeneboronic acid, m-carboxy-

CAS: 25487-66-5

Benzeneboronic acid, m-carboxy- is a bioactive chemical.

Formula: C₇H₇BO₄

Color and Shape: Off-White Crystalline Powder

Molecular weight: 165.94

Ref: TM-T21273

3-Carboxyphenylboronic Acid

Controlled Product

CAS: 25487-66-5

Applications 3-Carboxyphenylboronic Acid is used in phenylboronic acid-decorated gelatin nanoparticles for enhanced tumor targeting and penetration.
References Wang, X., et al.: Nanotechnology, 27, 385101 (2016); Wang, X., et al.: Eur. J. Pharm. Biopharm., 113, 168 (2017)

Formula: C₇H₇BO₄

Color and Shape: Off White

Molecular weight: 165.94

Ref: TR-C181383

3-Carboxybenzeneboronic acid

CAS: 25487-66-5

Formula: C₇H₇BO₄

Purity: 97%

Color and Shape: Solid, White to off-white solid

Molecular weight: 165.94

Ref: 10-F010785

3-Carboxyphenylboronic acid

CAS: 25487-66-5

3-Carboxyphenylboronic acid is a natural compound that is used in the treatment of tumors. It is also used as a starting material for the synthesis of other compounds, such as 3-carboxyphenylboronic acid and 3-carboxyphenylboronic acid hydrochloride. 3-Carboxyphenylboronic acid has been shown to activate signal pathways involved in tumor growth, survival, and metastasis. This drug has low bioavailability and can be excreted through urine or human serum. 3-Carboxyphenylboronic acid contains a pyrazole ring with ester linkages. Hydrogen bonding interactions are also present between this molecule and dopamine, which may account for its antitumor activity.

Formula: C₇H₇BO₄

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 165.94 g/mol

Ref: 3D-FC15977

3-Carboxybenzeneboronic Acid extrapure, 97%

CAS: 25487-66-5

Formula: C₇H₇BO₄

Purity: min. 97%

Color and Shape: White, Crystalline powder

Molecular weight: 165.9

Ref: SR-87379

Eltrombopag Impurity 11

CAS: 25487-66-5

Formula: C₇H₇BO₄

Molecular weight: 165.94

Ref: ST-EA-CP-E53020