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CAS 180576-11-8

:

2-[[2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]ethyl]thio]acetic acid

Description:
2-[[2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]ethyl]thio]acetic acid, commonly referred to as a protected amino acid derivative, is characterized by its complex structure that includes a fluorenylmethoxycarbonyl (Fmoc) group, which is widely used in peptide synthesis for protecting amino groups. The presence of a thioether linkage in its structure enhances its reactivity and solubility in organic solvents, making it suitable for various chemical reactions. This compound typically exhibits good stability under standard laboratory conditions, but it may be sensitive to strong acids or bases, which can lead to the cleavage of the Fmoc protecting group. Its molecular structure allows for potential applications in medicinal chemistry and biochemistry, particularly in the synthesis of peptides and other bioactive compounds. Additionally, the carboxylic acid functional group contributes to its acidic properties, influencing its behavior in solution and interactions with other molecules. Overall, this compound is valuable in synthetic organic chemistry, particularly in the context of peptide synthesis and modification.
Formula:C19H19NO4S
InChI:InChI=1S/C19H19NO4S/c21-18(22)12-25-10-9-20-19(23)24-11-17-15-7-3-1-5-13(15)14-6-2-4-8-16(14)17/h1-8,17H,9-12H2,(H,20,23)(H,21,22)
InChI key:InChIKey=ZXLLBDQWPUFJGL-UHFFFAOYSA-N
SMILES:C(OC(NCCSCC(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • 2-[[2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]ethyl]thio]acetic acid
  • 2-[[2-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)ethyl]sulfanyl]acetic acid
  • Acetic acid, 2-[[2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]ethyl]thio]-
  • Acetic acid, [[2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]ethyl]thio]-
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