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CAS 389889-80-9

:

1-Piperidinecarboxylicacid, 4-hydroxy-4-(hydroxymethyl)-, 1,1-dimethylethyl ester

Description:
1-Piperidinecarboxylic acid, 4-hydroxy-4-(hydroxymethyl)-, 1,1-dimethylethyl ester, identified by CAS number 389889-80-9, is an organic compound characterized by its piperidine ring structure, which contributes to its cyclic amine properties. This compound features a carboxylic acid functional group, indicating its potential acidity, alongside hydroxy and ester functionalities that suggest it may participate in hydrogen bonding and esterification reactions. The presence of the tert-butyl ester group enhances its lipophilicity, potentially influencing its solubility and bioavailability in various environments. The hydroxymethyl group adds to its reactivity and may serve as a site for further chemical modifications. Overall, this compound's unique structural features suggest it could have applications in medicinal chemistry or as an intermediate in organic synthesis, although specific biological activities or applications would require further investigation. Its stability, reactivity, and interactions with other molecules would depend on the surrounding conditions, such as pH and temperature.
Formula:C11H21NO4
InChI:InChI=1S/C11H21NO4/c1-10(2,3)16-9(14)12-6-4-11(15,8-13)5-7-12/h13,15H,4-8H2,1-3H3
InChI key:InChIKey=BKZFMSPPZXDTJL-UHFFFAOYSA-N
SMILES:C(O)C1(O)CCN(C(OC(C)(C)C)=O)CC1
Synonyms:
  • 1,1-Dimethylethyl 4-hydroxy-4-(hydroxymethyl)-1-piperidinecarboxylate
  • 1-Boc-4-hydroxy-4-(hydroxymethyl)-piperidine
  • 1-Piperidinecarboxylic acid, 4-hydroxy-4-(hydroxymethyl)-, 1,1-dimethylethyl ester
  • 4-Hydroxy-4-hydroxymethylpiperidine-1-carboxylic acid tert-butyl ester
  • Tert-Butyl 4-Hydroxy-4-(Hydroxymethyl)Piperidine-1-Carboxylate
  • tert-Butyl 4-hydroxy-4-(hydroxymethyl)tetrahydropyridine-1(2H)-carboxylate
  • tert-Butyl4-hydroxy-4-(hydroxymethyl)tetrahydropyridine-1(2H)-carboxylate
  • 1-Boc-4-hydroxy-4-(hydrox...
  • 1-Boc-4-(hydroxymethyl)piperidin-4-ol
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