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CAS 1218790-31-8

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1,1-Dimethylethyl 7-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate

Description:
1,1-Dimethylethyl 7-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate, with the CAS number 1218790-31-8, is a chemical compound characterized by its complex structure, which includes an indole moiety, a chloro substituent, and a boron-containing dioxaborolane group. This compound is likely to exhibit properties typical of indole derivatives, such as potential biological activity, including anti-cancer or anti-inflammatory effects, due to the presence of the indole ring, which is known for its role in various pharmacological applications. The presence of the boron-containing group may enhance its reactivity and solubility, making it suitable for specific synthetic applications or as a building block in organic synthesis. Additionally, the tert-butyl group (1,1-dimethylethyl) may contribute to the compound's stability and steric hindrance, influencing its interactions with biological targets or other chemical species. Overall, this compound's unique structural features suggest it may have specialized applications in medicinal chemistry or materials science.
Formula:C19H25BClNO4
InChI:InChI=1S/C19H25BClNO4/c1-17(2,3)24-16(23)22-11-13(12-9-8-10-14(21)15(12)22)20-25-18(4,5)19(6,7)26-20/h8-11H,1-7H3
InChI key:InChIKey=BEBXOCOXQGXHIB-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1C=2C(C(=C1)B3OC(C)(C)C(C)(C)O3)=CC=CC2Cl
Synonyms:
  • 1H-Indole-1-carboxylic acid, 7-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl 7-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
  • tert-Butyl 7-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
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