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CAS 1951440-97-3

:

1,1-Dimethylethyl 4-(5-bromo-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinecarboxylate

Description:
1,1-Dimethylethyl 4-(5-bromo-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinecarboxylate is a chemical compound characterized by its complex structure, which includes a piperidine ring and a benzimidazole moiety. The presence of the 5-bromo substituent indicates that it has halogen functionality, which can influence its reactivity and biological activity. The dimethyl group attached to the piperidine enhances steric hindrance, potentially affecting the compound's interaction with biological targets. This compound may exhibit properties typical of both piperidine derivatives and benzimidazole derivatives, such as potential pharmacological activities. Its carboxylate functionality suggests it may participate in various chemical reactions, including esterification or nucleophilic substitution. The compound's molecular weight, solubility, and stability would depend on its specific structural features and the presence of functional groups. Overall, this compound could be of interest in medicinal chemistry, particularly in the development of new therapeutic agents.
Formula:C17H22BrN3O3
InChI:InChI=1S/C17H22BrN3O3/c1-17(2,3)24-16(23)20-8-6-12(7-9-20)21-14-5-4-11(18)10-13(14)19-15(21)22/h4-5,10,12H,6-9H2,1-3H3,(H,19,22)
InChI key:InChIKey=UQSBDLJHHQFQDY-UHFFFAOYSA-N
SMILES:O=C1N(C=2C(N1)=CC(Br)=CC2)C3CCN(C(OC(C)(C)C)=O)CC3
Synonyms:
  • 1,1-Dimethylethyl 4-(5-bromo-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinecarboxylate
  • 1-Piperidinecarboxylic acid, 4-(5-bromo-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-, 1,1-dimethylethyl ester
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