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CAS 193693-62-8

:

(2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidineacetic acid

Description:
(2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidineacetic acid, with CAS number 193693-62-8, is a chemical compound characterized by its unique structure that includes a piperidine ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is often utilized in peptide synthesis as a building block due to the stability and protection offered by the Fmoc group, which can be selectively removed under basic conditions. The presence of the piperidine moiety contributes to its potential biological activity, as piperidine derivatives are known for their roles in various pharmacological applications. The compound is typically a white to off-white solid, soluble in organic solvents, and exhibits specific reactivity patterns typical of carboxylic acids and amines. Its stereochemistry, indicated by the (2S) designation, suggests that it has a specific spatial arrangement that may influence its interaction with biological targets. Overall, this compound is significant in the field of medicinal chemistry and peptide research.
Formula:C22H23NO4
InChI:InChI=1S/C22H23NO4/c24-21(25)13-15-7-5-6-12-23(15)22(26)27-14-20-18-10-3-1-8-16(18)17-9-2-4-11-19(17)20/h1-4,8-11,15,20H,5-7,12-14H2,(H,24,25)/t15-/m0/s1
InChI key:InChIKey=YVHXTQQJFAOBCJ-HNNXBMFYSA-N
SMILES:C(OC(=O)N1[C@H](CC(O)=O)CCCC1)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidineacetic acid
  • (S)-Fmoc-(2-Carboxymethyl)-Piperidine
  • 2-Piperidineacetic acid, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-, (2S)-
  • 2-Piperidineacetic acid, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-, (S)-
  • 2-[(2S)-1-[[(9H-Fluoren-9-yl)methoxy]carbonyl]piperidin-2-yl]acetic acid
  • (S)-(1-Fmoc-piperidin-2-yl)acetic acid
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