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CS-W001157 4
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Fmoc-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH

  • CAS No. 2264011-98-3

  • Cat. No. CS-0159204
  • Purity≥95%
  • MDL No.None

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

Fmoc-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH|CS-0159204

Structure of 2264011-98-3

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General Information

  • CAS No. 2264011-98-3
  • Cat. No. CS-0159204
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₃H₃₅N₅O₉
  • Molecular Weight 645.66
  • Synonym(s) None
  • SMILES OC(COCNC(CNC([C@H](CC1=CC=CC=C1)NC(CNC(CNC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)=O)=O)=O)=O)=O

Description

Fmoc-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH is a peptide derivative featuring a C-terminal ester-linked carboxylic acid, enabling efficient conjugation in bioconjugation workflows. The Fmoc group ensures orthogonal protection during solid-phase synthesis, while the glycine-rich sequence provides flexibility and solubility. This structure facilitates site-specific labeling and incorporation into larger biomolecular constructs under standard conditions.

Application

Fmoc-Gly-Gly-Phe-Gly-NH-CH₂-O-CH₂COOH serves as a well-defined peptide-based building block for the synthesis of cyclic or constrained peptide scaffolds. The Fmoc group enables efficient solid-phase peptide synthesis, while the C-terminal hydroxymethyl ester facilitates conjugation and derivatization. Its sequence incorporates orthogonal protection and stable linkages, offering reliable handling and purification in multi-step synthetic workflows.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   201.26
  • LogP   0.6599
  • H_Acceptors   8
  • H_Donors   6
  • Rotatable_Bonds   16

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