Nom du produit:(5-Bromopyridin-3-yl)boronic acid

IUPAC Name:(5-bromopyridin-3-yl)boronic acid

CAS:452972-09-7
Formule moléculaire:C5H5BBrNO2
Pureté:95%+
Numéro de catalogue:CM103400
Poids moléculaire:201.81

Unité d'emballage Stock disponible Prix($) Quantité
CM103400-100g in stock ƱȌȦ

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Détails du produit

N° CAS:452972-09-7
Formule moléculaire:C5H5BBrNO2
Point de fusion:-
Code SMILES:BrC1=CN=CC(B(O)O)=C1
Densité:
Numéro de catalogue:CM103400
Poids moléculaire:201.81
Point d'ébullition:
N° Mdl:MFCD02685634
Stockage:

Category Infos

Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.
Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Product Overview 5-Bromopyridine-3-boronic acid, also known as 5-BPBA, is an important organic compound in the field of organic chemistry. It is a boronic acid derivative.
Synthesis Method 5-Bromopyridine-3-boronic acid can be synthesized in several ways, but the most commonly used method is the reaction of 5-bromopyridine and 3-boronic acid. This reaction produces a highly reactive intermediate, which can be further converted into 5-Bromopyridine-3-boronic acid by a variety of methods. The most common method involves the use of a palladium catalyst and a base such as sodium bicarbonate. This method is simple and efficient, and can be used to synthesize 5-Bromopyridine-3-boronic acid in large quantities.
Chemical Properties 5-Bromopyridine-3-boronic acid is a highly reactive compound and can be easily synthesized in the laboratory. It is also relatively stable, making it suitable for use in a variety of experiments. However, it can be toxic in high doses, so it should be handled with care.
Synthesis and Application It is an important building block for organic synthesis and can be used to synthesize a variety of compounds, including drugs and other biologically active compounds. It has also been used in medicinal chemistry to study the structure and activity of various enzymes and receptors. In biochemistry, 5-Bromopyridine-3-boronic acid has been used to study the structure and function of proteins and nucleic acids.
Future Directions Further research is needed to better understand its mechanism of action and to develop new and more effective uses for this compound. Possible future directions for research include exploring its use in drug development, studying its effects on other enzymes and receptors, and exploring its potential as a therapeutic agent.