CAS 476004-79-2
:2-Pinacolateborylpyrrole
Description:
2-Pinacolateborylpyrrole is an organoboron compound characterized by the presence of a boron atom bonded to a pyrrole ring and a pinacolate group. This compound typically exhibits properties associated with both boron and nitrogen functionalities, making it of interest in various chemical applications, including organic synthesis and materials science. The boron atom in 2-Pinacolateborylpyrrole can participate in coordination chemistry, potentially forming complexes with other ligands. The pyrrole moiety contributes to the compound's electronic properties, often enhancing its reactivity and stability. Additionally, the pinacolate group, derived from pinacol, provides steric hindrance and can influence the solubility and reactivity of the compound. Overall, 2-Pinacolateborylpyrrole is notable for its potential applications in catalysis, organic electronics, and as a building block in the synthesis of more complex organic molecules. Its unique structural features and reactivity profile make it a subject of interest in contemporary chemical research.
Formula:C10H16BNO2
InChI:InChI=1/C10H16BNO2/c1-9(2)10(3,4)14-11(13-9)8-6-5-7-12-8/h5-7,12H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc[nH]2)O1
Synonyms:- 1H-pyrrole, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
- 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole
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Found 3 products.
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole
CAS:Formula:C10H16BNO2Color and Shape:SolidMolecular weight:193.05052-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole
CAS:Purity:95.0%Molecular weight:193.05000305175782-Pinacolateborylpyrrole
CAS:Controlled Product<p>Applications 2-Pinacolateborylpyrrole is a useful reagent for organic reactions.<br>References Pati, N.N., et al.: Eur. J. Org. Chem., 2017, 741-45 (2017); Kise, K., et al.: Chem. Lett., 46, 1319-22 (2017);<br></p>Formula:C10H16BNO2Color and Shape:NeatMolecular weight:193.05


