CAS 1692-25-7
:Pyridine-3-boronic acid
Description:
Pyridine-3-boronic acid, with the CAS number 1692-25-7, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring at the 3-position. 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. Pyridine-3-boronic acid is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. The boronic acid moiety can also participate in various reactions, including the formation of boronate esters and coordination with diols, making it valuable in medicinal chemistry and materials science. Additionally, its ability to form complexes with biomolecules has implications in biological applications. Overall, pyridine-3-boronic acid is a significant compound in both synthetic and applied chemistry due to its reactivity and functional versatility.
Formula:C5H6BNO2
InChI:InChI=1/C5H6BNO2/c8-6(9)5-2-1-3-7-4-5/h1-4,8-9H
InChI key:InChIKey=ABMYEXAYWZJVOV-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=CC=NC1
Synonyms:- (3-Pyridinyl)boronic acid
- (Pyridin-3-Yl)Boronic Acid
- 3-Pyridineboronic acid
- 3-Pyridinylboronic acid
- 3-Pyridylboronic acid
- B-3-Pyridinylboronic acid
- Boronic acid, 3-pyridinyl-
- Boronic acid, B-3-pyridinyl-
- Dihydroxy(3-pyridyl)borane
- Pyridin-3-Boronic Acid
- Pyridin-3-Ylboronic Acid
- Pyridin-3-Ylboronicacid
- Pyridine-3-boronic acidl
- Pyridine-3-boronicacid
- IFLAB-BB F1957-0039
- 3-Pridylboronic acid
- 3-PYRIDINEBORNIC ACID
- PYRIDINE-3-BORONIC ACID
- PYRIDYL-3-BORONIC ACID
- AKOS BRN-0272
- 3-Pyridylboronic Acid (contains varying amounts of Anhydride)
- 3-pyridineboric acid
- RARECHEM AH PB 0251
- Pyridine-3-boronic acid ,98%
- PYRIDIN-3-YL-3-BORONIC ACID
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Found 9 products.
Boronic acid, B-3-pyridinyl-
CAS:Formula:C5H6BNO2Purity:95%Color and Shape:SolidMolecular weight:122.91763-Pyridylboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C5H6BNO2Purity:97.0 to 117.0 %Color and Shape:White to Light yellow powder to crystalMolecular weight:122.92Pyridine-3-boronic acid
CAS:Pyridine-3-boronic acidFormula:C5H6BNO2Purity:95%Color and Shape: white powderMolecular weight:122.92g/molPyridine-3-boronic acid
CAS:Formula:C5H6BNO2Purity:95%Color and Shape:CrystallineMolecular weight:122.923-Pyridineboronic Acid
CAS:Controlled Product<p>Applications Boronic acid derivatives and their binding affinities with diols.<br>References Yang, W., et al.: Bioorg. Med. Chem. Lett., 12, 2175 (2002), Yang, W., et al.: Med. Res. Rev., 23, 346 (2003),<br></p>Formula:C5H6BNO2Color and Shape:NeatMolecular weight:122.923-Pyridineboronic Acid extrapure, 98%
CAS:Formula:C5H6BNO2Purity:min. 98.0%Color and Shape:White to off-white, Powder, ClearMolecular weight:122.923-Pyridineboronic acid
CAS:<p>3-Pyridineboronic acid is an antimicrobial agent that is used to treat bacterial and fungal infections. 3-Pyridineboronic acid is a prodrug that is metabolized to its active form, pyridinium boronate. This drug has been shown to be effective in the treatment of hypoxic tumors in mice, which are resistant to other anticancer drugs. 3-Pyridineboronic acid also has acidic properties and can be used as an antiseptic for the treatment of skin and eye infections. It can also be used as a hydrogen bonding partner when combined with halides, such as chloride or bromide ions. The drug binds to human serum proteins and forms an acidic complex that prevents bacterial growth by inhibiting protein synthesis. 3-Pyridineboronic acid also inhibits prostate cancer cells by competitively inhibiting the enzyme 4-pyridinylboronic acid reductase (4PBAR).</p>Formula:C5H6BNO2Purity:Min. 95%Molecular weight:122.92 g/mol
