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CAS 285996-74-9

:

1-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-oxocyclohexanecarboxylic acid

Description:
1-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-oxocyclohexanecarboxylic acid, commonly referred to as Fmoc-amino acid derivative, is a chemical compound characterized by its complex structure that includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, an amino group, and a cyclohexanecarboxylic acid moiety. This compound is typically used in peptide synthesis as a protecting group for amino acids, allowing for selective reactions without interfering with the amino functionality. The Fmoc group is known for its stability under basic conditions and can be removed under mild acidic conditions, making it advantageous in synthetic chemistry. The presence of the 4-oxocyclohexanecarboxylic acid component contributes to its reactivity and potential applications in drug development and materials science. Additionally, the compound's unique structure may influence its solubility, stability, and interaction with biological systems, making it a subject of interest in medicinal chemistry and biochemistry. Overall, this compound exemplifies the intricate design often required in the synthesis of biologically active molecules.
Formula:C22H21NO5
InChI:InChI=1S/C22H21NO5/c24-14-9-11-22(12-10-14,20(25)26)23-21(27)28-13-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-8,19H,9-13H2,(H,23,27)(H,25,26)
InChI key:InChIKey=SHBYYFRMCILKOK-UHFFFAOYSA-N
SMILES:C(OC(NC1(C(O)=O)CCC(=O)CC1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • 1-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)-4-oxocyclohexane-1-carboxylic acid
  • 1-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-oxocyclohexanecarboxylic acid
  • 1-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxocyclohexanecarboxylate
  • Cyclohexanecarboxylic acid, 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-oxo-
  • N-(9-Fluorenylmethoxycarbonyl)-amino-4-ketocyclohexylcarboxylic acid
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