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2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acid

  • CAS No. 219640-94-5

  • Cat. No. CS-0433436
  • Purity≥97%
  • MDL No.MFCD11226785

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

2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acid|CS-0433436

Structure of 219640-94-5

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General Information

  • CAS No. 219640-94-5
  • Cat. No. CS-0433436
  • Purity ≥97%
  • MDL No. MFCD11226785
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₃H₁₉NO₄
  • Molecular Weight 373.40
  • Synonym(s) FMoc-OaMb
  • SMILES O=C(O)C1=CC=CC=C1CNC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O

Description

This fluorenylmethoxycarbonyl-protected amino acid derivative features a benzyl side chain with a carboxylic acid group, enabling straightforward incorporation into peptide synthesis workflows. The C-terminal functionality supports efficient coupling reactions under standard conditions, while the fluorenylmethoxycarbonyl group provides robust protection and clean deprotection.

Application

2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acid serves as a robust, bench-stable amino acid derivative enabling efficient peptide synthesis. The Fmoc group provides orthogonal protection for amines with high stability under basic conditions and facile removal via mild acidolysis. The benzoic acid side chain offers a versatile handle for further functionalization, including amide coupling or derivatization, making it ideal for constructing complex peptide scaffolds and bioactive molecules in medicinal chemistry 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   75.63
  • LogP   4.4235
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   5

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