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CAS 1072946-29-2

:

1-(1,1-Dimethylethyl) 4-(4-borono-3-methoxyphenoxy)-1-piperidinecarboxylate

Description:
1-(1,1-Dimethylethyl) 4-(4-borono-3-methoxyphenoxy)-1-piperidinecarboxylate, with the CAS number 1072946-29-2, is a chemical compound characterized by its complex structure, which includes a piperidine ring, a boronic acid moiety, and a methoxy-substituted phenyl group. The presence of the tert-butyl group (1,1-dimethylethyl) contributes to its steric bulk, potentially influencing its reactivity and solubility. The boronic acid functionality is significant for its ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. The methoxy group enhances the compound's lipophilicity, which may affect its biological activity and interaction with cellular targets. Overall, this compound's unique combination of functional groups suggests potential utility in medicinal chemistry, particularly in the design of targeted therapies or as a building block in organic synthesis. Its specific properties, such as solubility and stability, would depend on the surrounding conditions and the presence of other functional groups in a given formulation.
Formula:C17H26BNO6
InChI:InChI=1S/C17H26BNO6/c1-17(2,3)25-16(20)19-9-7-12(8-10-19)24-13-5-6-14(18(21)22)15(11-13)23-4/h5-6,11-12,21-22H,7-10H2,1-4H3
InChI key:InChIKey=IKZNJZJEWBIUGX-UHFFFAOYSA-N
SMILES:O(C1=CC(OC)=C(B(O)O)C=C1)C2CCN(C(OC(C)(C)C)=O)CC2
Synonyms:
  • 1-(1,1-Dimethylethyl) 4-(4-borono-3-methoxyphenoxy)-1-piperidinecarboxylate
  • 1-Piperidinecarboxylic acid, 4-(4-borono-3-methoxyphenoxy)-, 1-(1,1-dimethylethyl) ester
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