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CS-W001157 4
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4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid

  • CAS No. 252206-28-3

  • Cat. No. CS-0044529
  • Molecule weightNone
  • Purity≥95%
  • MDL No.MFCD02259498

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

4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid|CS-0044529

Structure of 252206-28-3

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General Information

  • CAS No. 252206-28-3
  • Cat. No. CS-0044529
  • Purity ≥95%
  • MDL No. MFCD02259498
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₀H₁₇N₃O₄
  • Molecular Weight None
  • Synonym(s) 4-(Fmoc-amino)-1-methyl-1H-Imidazole-2-carboxylic Acid
  • SMILES O=C(C1=NC(NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)=CN1C)O

Description

This fluorenylmethoxycarbonyl-protected imidazole carboxylic acid integrates a sterically hindered, bench-stable imidazole moiety with a cleavable Fmoc group, enabling efficient incorporation into peptide chains under standard coupling conditions.

Application

4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid serves as a robust, bench-stable amino acid building block for peptide synthesis, enabling efficient N-terminal protection and orthogonal deprotection under mild conditions. The Fmoc group facilitates selective coupling in solid-phase workflows, while the imidazole-2-carboxylic acid moiety provides a versatile handle for conjugation and scaffold elaboration in medicinal chemistry applications.

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-H320-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   93.45
  • LogP   3.4793
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   4

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