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CAS 917099-02-6

:

rel-1-(9H-Fluoren-9-ylmethyl) (2R,4S)-4-hydroxy-1,2-piperidinedicarboxylate

Description:
Rel-1-(9H-Fluoren-9-ylmethyl) (2R,4S)-4-hydroxy-1,2-piperidinedicarboxylate is a chemical compound characterized by its complex structure, which includes a piperidine ring substituted with hydroxyl and carboxylate groups, as well as a fluorenylmethyl moiety. This compound is typically used in medicinal chemistry and drug development due to its potential biological activity. The presence of the hydroxyl group suggests it may participate in hydrogen bonding, influencing its solubility and reactivity. The stereochemistry indicated by the (2R,4S) configuration is crucial for its biological interactions, as chirality can significantly affect the pharmacological properties of compounds. Additionally, the fluorenylmethyl group may enhance lipophilicity, potentially improving membrane permeability. The compound's CAS number, 917099-02-6, allows for precise identification in chemical databases, facilitating research and development efforts. Overall, this substance exemplifies the intricate relationship between molecular structure and biological function in the field of organic and medicinal chemistry.
Formula:C21H21NO5
InChI:InChI=1/C21H21NO5/c23-13-9-10-22(19(11-13)20(24)25)21(26)27-12-18-16-7-3-1-5-14(16)15-6-2-4-8-17(15)18/h1-8,13,18-19,23H,9-12H2,(H,24,25)/t13-,19+/s2
InChI key:InChIKey=CJGSLUBWMLBOFZ-KINVLMLONA-N
SMILES:C(OC(=O)N1[C@H](C(O)=O)C[C@H](O)CC1)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • 1,2-Piperidinedicarboxylic acid, 4-hydroxy-, 1-(9H-fluoren-9-ylmethyl) ester, (2R,4S)-rel-
  • rel-1-(9H-Fluoren-9-ylmethyl) (2R,4S)-4-hydroxy-1,2-piperidinedicarboxylate
  • rel-(2R,4S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-hydroxypiperidine-2-carboxylic acid
  • (2R,4S)-1-(((9H-Fluoren-9-yl)Methoxy)carbonyl)-4-hydroxypiperidine-2-carboxylic acid
  • (2R,4S)-FMOC-4-HYDROXYPIPERIDINE-2-CARBOXYLIC ACID
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