CAS 191171-55-8
:2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Description:
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, with the CAS number 191171-55-8, is an organic compound characterized by the presence of both an aniline group and a boron-containing dioxaborolane moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. The dioxaborolane structure contributes to its reactivity, particularly in cross-coupling reactions, making it valuable in synthetic organic chemistry, especially in the formation of carbon-carbon bonds. The presence of the tetramethyl substituents enhances its stability and solubility, while the aniline part provides potential for further functionalization. Additionally, this compound may exhibit interesting electronic properties due to the conjugation between the aniline and the boron-containing group, which can influence its behavior in various chemical environments. Overall, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile building block in the synthesis of complex organic molecules.
Formula:C12H18BNO2
InChI:InChI=1S/C12H18BNO2/c1-11(2)12(3,4)16-13(15-11)9-7-5-6-8-10(9)14/h5-8H,14H2,1-4H3
InChI key:InChIKey=ZCJRWQDZPIIYLM-UHFFFAOYSA-N
SMILES:NC1=C(B2OC(C)(C)C(C)(C)O2)C=CC=C1
Synonyms:- 2-(2-Aminophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
- 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine
- 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenylamine
- 2-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
- 2-Aminobenzeneboronic acid pinacol cyclic ester
- 2-Aminophenylboronic acid pinacol cyclic ester
- 2-Aminophenylboronic acid pinacol ester
- Benzenamine, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
- 2-Aminophenyl boronic acid pinacol ester
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Found 8 products.
2-Aminobenzeneboronic acid pinacol ester, 97%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C12H18BNO2Purity:97%Color and Shape:White to cream to brown, Crystalline powderMolecular weight:219.09Benzenamine, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:Formula:C12H18BNO2Purity:97%Color and Shape:SolidMolecular weight:219.08782-(Aminophenyl)boronic acid, pinacol ester
CAS:<p>2-(Aminophenyl)boronic acid, pinacol ester</p>Formula:C12H18BNO2Purity:98%Color and Shape: off white solidMolecular weight:219.09g/mol2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS:Formula:C12H18BNO2Purity:>98.0%(GC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:219.092-Aminophenylboronic acid pinacol cyclic ester
CAS:<p>This compound is a drug target that is an organic molecule found in many pharmaceuticals. It is an acidic, ammonium persulfate-sensitive biomolecule, which can be introduced into cells and tissues to study their function. This compound has been shown to have cancer-fighting abilities, and has potent inhibitory activity against microbial infections. The compound also has suzuki coupling properties, which are used to introduce hemicyanine groups onto other molecules.</p>Formula:C12H18BNO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:219.09 g/mol2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS:Formula:C12H18BNO2Purity:97%Color and Shape:SolidMolecular weight:219.092-Aminobenzeneboronic acid pinacol ester
CAS:Controlled Product<p>Applications 2-Aminobenzeneboronic acid pinacol ester is a reagent used to synthesize regiospecific quinolines. It can also be used to synthesize (±)-Epimeloscine and (±)-Meloscine.<br>References Zhang, H., et al.: J. Am. Chem. Soc. 133, 10376 (2011); Horn, J., et al.: Org. Lett 10, 4117 (2008)<br></p>Formula:C12H20BNO3Color and Shape:NeatMolecular weight:237.103







