CAS 197958-29-5
:2-Pyridineboronic acid
Description:
2-Pyridineboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. It typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols. The compound features a boron atom bonded to a hydroxyl group and a pyridine ring, which contributes to its reactivity and utility in various chemical applications. 2-Pyridineboronic acid is known for its role in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. Additionally, it can act as a ligand in coordination chemistry and has potential applications in medicinal chemistry due to its ability to interact with biological molecules. The compound's reactivity is influenced by the electron-withdrawing nature of the pyridine ring, which can enhance its electrophilic properties. Overall, 2-pyridineboronic acid is a versatile reagent in synthetic organic chemistry, with implications in both industrial and research settings.
Formula:C5H6BNO2
InChI:InChI=1/C5H6BNO2/c8-6(9)5-3-1-2-4-7-5/h1-4,8-9H
SMILES:c1ccnc(c1)B(O)O
Synonyms:- Pyridin-2-Ylboronic Acid
- Pyridin-2-Yl-2-Boronic Acid
- Pyridine-2-Boronic Acid
- 2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
- 2-Pyridinebornic Acid
- 2-Pyridinylboronic Acid
- Boronic acid, 2-pyridinyl- (9CI)
- 2-Pyridylboronic Acid
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Found 6 products.
Pyridine-2-boronic acid, 95%
CAS:<p>Pyridine-2-boronic acid is used as a key starting material for the formation of pyridyl boronic ester such as pyridine-2-boronic acid dimethyl ester. Furthermore, the dimethyl ester reacts with bromquinoline to prepare the 2-pyridyl derivative of quinoline. This Thermo Scientific Chemicals brand pro</p>Formula:C5H6BNO2Purity:95%Molecular weight:122.922-Pyridineboronic Acid
CAS:Controlled ProductFormula:C5H6BNO2Color and Shape:NeatMolecular weight:122.9182-Pyridineboronic acid
CAS:<p>2-Pyridineboronic acid is a chemical compound that belongs to the group of quinoline derivatives. It is used in pharmaceutical preparations, including as an intermediate for the synthesis of other compounds. 2-Pyridineboronic acid has been shown to have antiproliferative effects on cancer cells and has been found to be active against nicotinic acetylcholine receptors (NAR). The compound also inhibits lipid kinase activity, which is involved in the production of phosphatidylcholine and phosphatidylethanolamine from phosphatidylserine. 2-Pyridineboronic acid can react with hydrochloric acid and electrochemical impedance spectroscopy to produce a solution that has a detection time of about 10 minutes.</p>Formula:C5H6BNO2Purity:Min. 95%Molecular weight:122.92 g/molBoronic acid, B-2-pyridinyl-
CAS:Formula:C5H6BNO2Purity:98%Color and Shape:SolidMolecular weight:122.9176





