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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-[[(2-phenylacetyl)amino]methyl]-L-cysteine

  • CAS No. 159680-21-4

  • Cat. No. CS-0162111
  • Purity≥98%
  • MDL No.MFCD18427303

*For research and further manufacturing use only, not for direct human use.

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-[[(2-phenylacetyl)amino]methyl]-L-cysteine|CS-0162111

Structure of 159680-21-4

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General Information

  • CAS No. 159680-21-4
  • Cat. No. CS-0162111
  • Purity ≥98%
  • MDL No. MFCD18427303
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₇H₂₆N₂O₅S
  • Molecular Weight 490.57
  • Synonym(s) N-(((9H-fluoren-9-yl)methoxy)carbonyl)-S-((2-phenylacetamido)methyl)-L-cysteine
  • SMILES O=C(O)[C@H](CSCNC(CC1=CC=CC=C1)=O)NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O

Description

Fmoc-S-[[(2-phenylacetyl)amino]methyl]-L-cysteine is a specialized cysteine derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group and a phenylacetyl-modified side chain. This configuration enables selective incorporation in solid-phase peptide synthesis, where the Fmoc moiety facilitates orthogonal deprotection. The modified thiol group supports site-specific conjugation strategies in chemical biology applications.

Application

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-[[(2-phenylacetyl)amino]methyl]-L-cysteine serves as a protected cysteine building block for peptide synthesis, enabling site-specific incorporation of thiol-containing residues. The Fmoc group provides orthogonal protection for the amine, while the phenylacetyl side chain offers enhanced stability and compatibility with standard deprotection protocols. Its well-defined reactivity facilitates efficient coupling and purification in solid-phase and solution-phase workflows, supporting scalable synthesis of complex peptides and heterocyclic scaffolds.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   104.73
  • LogP   4.0279
  • H_Acceptors   5
  • H_Donors   3
  • Rotatable_Bonds   10

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