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CAS 736990-02-6

:

ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylate

Description:
Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylate is a chemical compound characterized by its complex structure, which includes an indole moiety and a boron-containing dioxaborolane group. This compound typically exhibits properties associated with both the indole and boron functionalities, such as potential reactivity in organic synthesis and applications in medicinal chemistry. The presence of the ethyl ester group suggests it may have moderate solubility in organic solvents and could participate in various chemical reactions, including esterification and nucleophilic substitutions. Additionally, the boron atom in the dioxaborolane ring may facilitate unique reactivity patterns, making it useful in cross-coupling reactions or as a boron source in organic transformations. The compound's specific applications may include roles in drug development or as intermediates in the synthesis of more complex molecules. As with many organic compounds, handling should be done with care, considering potential toxicity and reactivity.
Formula:C17H22BNO4
InChI:InChI=1/C17H22BNO4/c1-6-21-15(20)14-10-11-9-12(7-8-13(11)19-14)18-22-16(2,3)17(4,5)23-18/h7-10,19H,6H2,1-5H3
SMILES:CCOC(=O)c1cc2cc(ccc2[nH]1)B1OC(C)(C)C(C)(C)O1
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