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CAS 368866-09-5

:

4-Piperidinecarboxylic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, hydrochloride (1:1)

Description:
4-Piperidinecarboxylic acid, 4-[[[9H-fluoren-9-ylmethoxy]carbonyl]amino]-, hydrochloride (1:1), commonly referred to as a protected amino acid derivative, is characterized by its structural complexity, featuring a piperidine ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is typically utilized in peptide synthesis, particularly in solid-phase synthesis, due to its stability and ease of removal of the Fmoc group under mild basic conditions. The hydrochloride salt form enhances its solubility in aqueous solutions, making it suitable for various biochemical applications. The presence of the piperidine moiety contributes to its basicity and potential interactions in biological systems. Additionally, the compound's molecular structure allows for specific steric and electronic properties, which can influence its reactivity and interactions with other molecules. Overall, this substance is valuable in synthetic organic chemistry and biochemistry, particularly in the development of peptide-based therapeutics.
Formula:C21H22N2O4·ClH
InChI:InChI=1S/C21H22N2O4.ClH/c24-19(25)21(9-11-22-12-10-21)23-20(26)27-13-18-16-7-3-1-5-14(16)15-6-2-4-8-17(15)18;/h1-8,18,22H,9-13H2,(H,23,26)(H,24,25);1H
InChI key:InChIKey=UDBFKLWITSYZJD-UHFFFAOYSA-N
SMILES:C(OC(NC1(C(O)=O)CCNCC1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3.Cl
Synonyms:
  • 4-Piperidinecarboxylic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, hydrochloride (1:1)
  • 4-Piperidinecarboxylic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, monohydrochloride
  • 4-Piperidinecarboxylicacid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, monohydrochloride (9CI)
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