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651030-57-8

Benzenepropanol, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

Catalog#: AR00IC5E  |   CAS#: 651030-57-8  |   MDL#: MFCD18734359  |   MF: C15H23BO3  |   MW: 262.1523

Packsize Purity Price Availability Quantity
100mg 97% $10.00 Global Stock Buy Now Add To Cart
250mg 97% $16.00 Global Stock Buy Now Add To Cart
1g 97% $55.00 Global Stock Buy Now Add To Cart
5g 97% $203.00 Global Stock Buy Now Add To Cart
10g 97% $404.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00IC5E
Chemical Name Benzenepropanol, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS Number 651030-57-8
Molecular Formula C15H23BO3
Molecular Weight 262.1523
MDL Number MFCD18734359
SMILES OCCCc1ccc(cc1)B1OC(C(O1)(C)C)(C)C

The compound 3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-1-ol has significant utility in chemical synthesis as a versatile building block. It serves as a key component in the synthesis of various organic molecules, particularly in the field of medicinal chemistry and material science.One important application of this compound lies in its role as a boron-containing reagent in Suzuki-Miyaura coupling reactions. In this process, the boron atom facilitates the coupling of aromatic or heteroaromatic compounds with organohalides or pseudohalides under palladium catalysis. This reaction is widely used in the synthesis of pharmaceuticals, agrochemicals, and functional materials.Furthermore, 3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-1-ol can also be employed in the preparation of chiral ligands for asymmetric catalysis. By tailoring the structure of this compound, chemists can design ligands that enhance the enantioselectivity of various chemical transformations, enabling the synthesis of optically pure compounds with high efficiency and selectivity.Overall, the unique structural features of 3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-1-ol make it a valuable tool in modern organic synthesis, allowing chemists to access diverse molecular scaffolds and conduct complex transformations with precision and control.
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