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

Pyridine-3-boronic acid

CAS: 1692-25-7

Pyridine-3-boronic acid

Formula: C₅H₆BNO₂

Purity: 95%

Color and Shape: White Solid-Powder

Molecular weight: 122.91764

Ref: 54-OR4119

Boronic acid, B-3-pyridinyl-

CAS: 1692-25-7

Formula: C₅H₆BNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 122.9176

Ref: IN-DA001YKM

Pyridine-3-boronic acid hydrochloride

CAS: 1692-25-7

Formula: C₅H₆BNO₂

Molecular weight: 122.92

Ref: 7W-GK8268

3-Pyridylboronic Acid (contains varying amounts of Anhydride)

CAS: 1692-25-7

Formula: C₅H₆BNO₂

Purity: 97.0 to 117.0 %

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 122.92

Ref: 3B-P1673

Pyridine-3-boronic acid

CAS: 1692-25-7

Purity: 95%

Molecular weight: 122.92

Ref: FT-P5775

Pyridin-3-ylboronic acid

CAS: 1692-25-7

Pyridin-3-ylboronic acid

Formula: C₅H₆BNO₂

Purity: 95%

Molecular weight: 122.92

Ref: IN-DG2713

Pyridine-3-boronic acid

CAS: 1692-25-7

Formula: C₅H₆BNO₂

Purity: 95%

Color and Shape: Crystalline

Molecular weight: 122.92

Ref: 10-F010819

3-Pyridineboronic Acid

Controlled Product

CAS: 1692-25-7

Applications Boronic acid derivatives and their binding affinities with diols.
References Yang, W., et al.: Bioorg. Med. Chem. Lett., 12, 2175 (2002), Yang, W., et al.: Med. Res. Rev., 23, 346 (2003),

Formula: C₅H₆BNO₂

Color and Shape: Neat

Molecular weight: 122.92

Ref: TR-P991350

3-Pyridineboronic Acid extrapure, 98%

CAS: 1692-25-7

Formula: C₅H₆BNO₂

Purity: min. 98.0%

Color and Shape: White to off-white, Powder, Clear

Molecular weight: 122.92

Ref: SR-73512

3-Pyridineboronic acid

CAS: 1692-25-7

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).

Formula: C₅H₆BNO₂

Purity: Min. 95%

Molecular weight: 122.92 g/mol

Ref: 3D-FP27301