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1256359-15-5

1H-Pyrazole, 1-(1,1-dimethylethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

Catalog#: AR000OV3  |   CAS#: 1256359-15-5  |   MDL#: MFCD16660302  |   MF: C13H23BN2O2  |   MW: 250.1449

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Catalog Number AR000OV3
Chemical Name 1H-Pyrazole, 1-(1,1-dimethylethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS Number 1256359-15-5
Molecular Formula C13H23BN2O2
Molecular Weight 250.1449
MDL Number MFCD16660302
SMILES CC1(C)OB(OC1(C)C)c1cnn(c1)C(C)(C)C 

1-(tert-Butyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, commonly referred to as $name$, serves as a versatile reagent in chemical synthesis. This compound is widely utilized in organic chemistry for the functionalization of aromatic compounds through C-H activation reactions. By acting as a directing group, $name$ enables selective ortho-C-H bond activation, facilitating the introduction of diverse functional groups with high regioselectivity.Moreover, $name$ plays a crucial role in the synthesis of biologically active molecules and pharmaceutical intermediates. Its unique structure containing a boronate ester moiety offers an efficient pathway for the installation of boron functionalities onto aromatic rings, which are key motifs in various drug discovery processes. The presence of a bulky tert-butyl group on the pyrazole ring enhances the stability and reactivity of the compound, making it a valuable building block in the design and synthesis of complex organic molecules.Overall, the application of 1-(tert-Butyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in chemical synthesis offers chemists a powerful tool for site-selective functionalization and molecular diversification, opening new possibilities for the efficient construction of novel compounds with tailored properties and biological activities.
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