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CAS 273222-04-1

:

(αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pyridinebutanoic acid

Description:
The chemical substance known as (αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pyridinebutanoic acid, with the CAS number 273222-04-1, is a synthetic compound primarily used in the field of medicinal chemistry and peptide synthesis. This compound features a pyridine ring, which contributes to its aromatic properties, and a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly utilized in the protection of amino acids during peptide synthesis. The presence of the carboxylic acid functional group indicates that it can participate in acid-base reactions, while the amino group suggests potential for forming peptide bonds. The stereochemistry indicated by (αS) suggests that it has specific spatial arrangements that may influence its biological activity and interactions. Overall, this compound is characterized by its complex structure, which combines elements of aromatic chemistry with functional groups relevant to biological applications, making it a valuable tool in drug development and research.
Formula:C24H22N2O4
InChI:InChI=1S/C24H22N2O4/c27-23(28)22(10-9-16-11-13-25-14-12-16)26-24(29)30-15-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-8,11-14,21-22H,9-10,15H2,(H,26,29)(H,27,28)/t22-/m0/s1
InChI key:InChIKey=FKBUYAZUIRMSJK-QFIPXVFZSA-N
SMILES:C(OC(N[C@@H](CCC=1C=CN=CC1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pyridinebutanoic acid
  • 4-Pyridinebutanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-
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