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N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N2-(2-((5-sulfonaphthalen-1-yl)amino)ethyl)-L-glutamine

  • CAS No. 193475-66-0

  • Cat. No. CS-0101101
  • Purity≥97%
  • MDL No.MFCD01076138

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

N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N2-(2-((5-sulfonaphthalen-1-yl)amino)ethyl)-L-glutamine|CS-0101101

Structure of 193475-66-0

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General Information

  • CAS No. 193475-66-0
  • Cat. No. CS-0101101
  • Purity ≥97%
  • MDL No. MFCD01076138
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₂H₃₁N₃O₈S
  • Molecular Weight 617.67
  • Synonym(s) None
  • SMILES O=C(N[C@@H](CCC(NCCNC1=CC=CC2=C1C=CC=C2S(=O)(O)=O)=O)C(O)=O)OCC3C4=C(C5=C3C=CC=C5)C=CC=C4

Description

N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N2-(2-((5-sulfonaphthalen-1-yl)amino)ethyl)-L-glutamine features a fluorenylmethoxycarbonyl group for robust N-terminal protection and a sulfonaphthalene-containing side chain that imparts high solubility and polarity. This combination enables efficient incorporation into peptide synthesis workflows, particularly for polar or charged sequences.

Application

N₂-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N₂-(2-((5-sulfonaphthalen-1-yl)amino)ethyl)-L-glutamine serves as a protected glutamine derivative enabling selective peptide synthesis via standard Fmoc-based coupling protocols. The fluorenylmethoxycarbonyl (Fmoc) group ensures efficient orthogonal deprotection, while the sulfonaphthylamino side chain provides enhanced solubility and stability in aqueous media. This compound functions as a valuable building block for constructing biologically relevant scaffolds, particularly in the context of enzyme inhibitor design and peptidomimetic development.

Safety Information

Download SDS
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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   171.13
  • LogP   4.3867
  • H_Acceptors   7
  • H_Donors   5
  • Rotatable_Bonds   12

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