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CAS 1335206-40-0

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Glycine, N-[2-[[(9H-fluoren-9-ylMethoxy)carbonyl]aMino]ethyl]-N-(Methylsulfonyl)-

Description:
Glycine, N-[2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]ethyl]-N-(methylsulfonyl)-, commonly referred to as a protected amino acid derivative, is characterized by its unique structure that includes a glycine backbone modified with a fluorenylmethoxycarbonyl (Fmoc) protecting group and a methylsulfonyl substituent. This compound is typically utilized in peptide synthesis due to the stability of the Fmoc group under basic conditions, allowing for selective deprotection during the synthesis process. The presence of the methylsulfonyl group enhances its solubility in polar solvents and may influence its reactivity and interaction with biological systems. Glycine itself is the simplest amino acid, and its derivatives often exhibit important roles in biochemistry and medicinal chemistry. The compound's molecular structure contributes to its potential applications in drug development and as a building block in the synthesis of more complex peptides. As with many synthetic compounds, careful handling and consideration of safety data are essential during its use in laboratory settings.
Formula:C20H22N2O6S
Synonyms:
  • ({3-[(9H-fluoren-9-ylmethoxycarbonylmethyl)-amino]-propyl}-methanesulfonyl-amino)-acetic acid
  • 2-{N-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)ethyl]methanesulfonamido}acetic acid
  • 2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl-methylsulfonylamino]acetic acid
  • N-[2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]-amino]ethyl]-N-(methylsulfonyl)-glycine
  • Glycine, N-[2-[[(9H-fluoren-9-ylMethoxy)carbonyl]aMino]ethyl]-N-(Methylsulfonyl)-
  • 2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)methylsulfonamido)acetic acid
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