CAS 89878-14-8
:3-(Diethylboryl)pyridine
Description:
3-(Diethylboryl)pyridine is an organoboron compound characterized by the presence of a pyridine ring substituted with a diethylboryl group. This compound typically exhibits properties associated with both boron and nitrogen functionalities, making it a valuable intermediate in organic synthesis and materials science. The diethylboryl group contributes to its reactivity, particularly in cross-coupling reactions and as a potential ligand in coordination chemistry. The pyridine moiety provides basicity and can participate in hydrogen bonding, influencing the compound's solubility and interaction with other molecules. Additionally, 3-(Diethylboryl)pyridine may exhibit unique optical properties due to the presence of the boron atom, which can affect its electronic structure. Its applications may extend to catalysis, organic electronics, and the development of new materials. Safety considerations should be taken into account when handling this compound, as organoboron compounds can be sensitive to moisture and air, potentially leading to hydrolysis or oxidation.
Formula:C9H14BN
InChI:InChI=1/C9H14BN/c1-3-10(4-2)9-6-5-7-11-8-9/h5-8H,3-4H2,1-2H3
InChI key:InChIKey=OJKBCQOJVMAHDX-UHFFFAOYSA-N
SMILES:B(CC)(CC)C=1C=CC=NC1
Synonyms:- 3-(Diethylboranyl)Pyridine
- 3-(Diethylboryl)Pyridine
- 3-Diethylboropyridine
- 3-Pyridinyldiethylborane
- 3-Pyridyldiethyl borane
- 3-Pyridyldiethylborane
- Abiraterone interMediate
- Debp
- Diethyl(3-(4-Pyridin-3-yl) borane
- Diethyl(3-Pyridinyl)-Borane
- Diethyl-(pyridin-3-yl)-borane
- Diethyl-3-pyridylborane
- Dithyl(3-pyridyl)Borane
- Pyridine, 3-(diethylboryl)-
- See more synonyms
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Found 10 products.
Diethyl(3-pyridyl)borane
CAS:Formula:C9H14BNPurity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:147.03Diethyl(3-pyridyl)borane, 98%
CAS:<p>Reactant for: preparation of inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents, N-Methylation reactions of the pyridyl group, Palladium catalyzed amination reactions, intramolecular Heck reactions, Coupling reactions and Synthesis of tri</p>Formula:C9H14BNPurity:98%Molecular weight:147.03Diethyl-(3-pyridyl)borane
CAS:<p>Diethyl-(3-pyridyl)borane</p>Formula:C9H14BNPurity:98%Color and Shape: white solidMolecular weight:147.03g/mol3-(Diethylboryl)pyridine
CAS:Controlled Product<p>Impurity Abiraterone Impurity 7<br>Applications 3-(Diethylboryl)pyridine is an intermediate used to prepare inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents. It is also used in the synthesis of trisubstituted pyrimidines from polyhalopyrimidines via Suzuki coupling.<br>References Charrier, J., et al.; J. Med. Pharm. Chem., 54, 2320 (2011); Large, J., et al.: Synlett., 861 (2006)<br></p>Formula:C9H14BNColor and Shape:NeatMolecular weight:147.023-(Diethylboryl) pyridine
CAS:<p>3-(Diethylboryl) pyridine is a halogenated biphenyl. It is used in the synthesis of 3-aryl substituted pyridines by cross-coupling reactions with aryl iodides, bromides and chlorides. Cross-coupling reactions are usually carried out at low temperatures (0 to 20°C) in order to minimize side reactions. The reaction is usually conducted in a biphasic system containing an organic solvent and water, which facilitates the extraction of the product from the mixture. 3-(Diethylboryl) pyridine reacts with halide ions via an electrophilic substitution reaction to form a reactive intermediate, which reacts with palladium catalyst to produce the desired product. This process is also called catalytic hydrogenation. 3-(Diethylboryl) pyridine has been shown to inhibit human cytochrome P450 enzymes, which are involved in drug metabolism and break down drugs</p>Formula:C9H14BNPurity:Min. 95%Color and Shape:PowderMolecular weight:147.03 g/mol
