AE20268
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $85.00 | $60.00 | - + | |
1g | 98% | in stock | $217.00 | $152.00 | - + | |
5g | 98% | in stock | $857.00 | $600.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE20268 |
Chemical Name: | 4-Methylindole-2-boronic acid pinacol ester |
CAS Number: | 1072811-23-4 |
Molecular Formula: | C15H20BNO2 |
Molecular Weight: | 257.1358 |
MDL Number: | MFCD11858397 |
SMILES: | Cc1cccc2c1cc([nH]2)B1OC(C(O1)(C)C)(C)C |
Complexity: | 342 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 19 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 1 |
4-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a versatile compound commonly employed in chemical synthesis for a variety of applications. In organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure containing both an indole moiety and a boronic ester group allows for strategic derivatization and functionalization through Suzuki-Miyaura cross-coupling reactions. This facilitates the construction of complex molecular architectures with high efficiency and selectivity. Additionally, 4-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole has found utility in the development of fluorescent probes, optoelectronic materials, and ligands for catalysis due to its tunable electronic properties and versatile reactivity. Its significance in chemical synthesis lies in its ability to enable the rapid assembly of structurally diverse compounds with enhanced biological or physicochemical properties for various scientific and industrial applications.