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4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,2-dimethylbutanoic acid

CAS 1310680-24-0: 4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,2-dimethylbutanoic acid

Description:4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,2-dimethylbutanoic acid, with CAS number 1310680-24-0, is a synthetic organic compound commonly used in peptide synthesis and as a protecting group in organic chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) group, which is a widely utilized protective group for amino acids, allowing for selective reactions without interfering with the amine functionality. The presence of the dimethylbutanoic acid moiety contributes to its hydrophobic characteristics, influencing solubility and reactivity. The compound is typically solid at room temperature and may exhibit moderate stability under standard conditions. Its structure includes both hydrophobic and polar regions, which can affect its interactions in biological systems. Additionally, the compound's synthesis and handling require careful consideration of safety protocols due to potential reactivity and toxicity associated with its components. Overall, this compound is significant in the field of medicinal chemistry and peptide research, facilitating the development of various bioactive molecules.

Formula:C21H23NO4

InChI:InChI=1S/C21H23NO4/c1-21(2,19(23)24)11-12-22-20(25)26-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h3-10,18H,11-13H2,1-2H3,(H,22,25)(H,23,24)

InChI key:InChIKey=JNYZWIAAJJHSFW-UHFFFAOYSA-N

SMILES:O=C(OCC1C=2C=CC=CC2C=3C=CC=CC31)NCCC(C(=O)O)(C)C

  • Synonyms:
  • Butanoic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2,2-dimethyl-
  • 4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,2-dimethylbutanoic acid
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4-({[(9H-Fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylbutanoic acid

CAS:1310680-24-0

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