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)
- See more synonyms
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Found 10 products.
3-Carboxyphenylboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C7H7BO4Purity:97.0 to 112.0 %Color and Shape:White to Orange to Green powder to crystalMolecular weight:165.943-Carboxybenzeneboronic acid
CAS:<p>3-Carboxybenzeneboronic acid</p>Formula:C7H7BO4Purity:≥95%Color and Shape: white to off-white solidMolecular weight:165.94g/molBenzeneboronic acid, m-carboxy-
CAS:<p>Benzeneboronic acid, m-carboxy- is a bioactive chemical.</p>Formula:C7H7BO4Color and Shape:Off-White Crystalline PowderMolecular weight:165.943-Carboxyphenylboronic Acid
CAS:Controlled Product<p>Applications 3-Carboxyphenylboronic Acid is used in phenylboronic acid-decorated gelatin nanoparticles for enhanced tumor targeting and penetration.<br>References Wang, X., et al.: Nanotechnology, 27, 385101 (2016); Wang, X., et al.: Eur. J. Pharm. Biopharm., 113, 168 (2017)<br></p>Formula:C7H7BO4Color and Shape:Off WhiteMolecular weight:165.943-Carboxybenzeneboronic acid
CAS:Formula:C7H7BO4Purity:97%Color and Shape:Solid, White to off-white solidMolecular weight:165.943-Carboxyphenylboronic acid
CAS:<p>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.</p>Formula:C7H7BO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:165.94 g/mol3-Carboxybenzeneboronic Acid extrapure, 97%
CAS:Formula:C7H7BO4Purity:min. 97%Color and Shape:White, Crystalline powderMolecular weight:165.9
