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CAS 273222-02-9

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

Description:
α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pyridinebutanoic acid, commonly referred to as Fmoc-4-pyridinebutanoic acid, is a chemical compound characterized by its structure, which includes a pyridine ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is primarily used in peptide synthesis as a building block, where the Fmoc group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis process. The presence of the pyridine moiety contributes to its unique chemical properties, including potential interactions with other molecules due to its nitrogen atom, which can participate in hydrogen bonding or coordination. The compound is typically solid at room temperature and is soluble in organic solvents, making it suitable for various synthetic applications. Its stability and reactivity are influenced by the functional groups present, which can be manipulated to facilitate the formation of peptide bonds or other chemical transformations. Overall, Fmoc-4-pyridinebutanoic acid is a valuable intermediate in the field of organic and medicinal chemistry.
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)
InChI key:InChIKey=FKBUYAZUIRMSJK-UHFFFAOYSA-N
SMILES:C(OC(NC(CCC=1C=CN=CC1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • 4-Pyridinebutanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-
  • α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pyridinebutanoic acid
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