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CS-W001157 4
Total: USD 88.00

4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-carboxyethyl)heptanedioic acid

  • CAS No. 798576-99-5

  • Cat. No. CS-0539103
  • Purity≥98%
  • MDL No.None

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

4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-carboxyethyl)heptanedioic acid|CS-0539103

Structure of 798576-99-5

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General Information

  • CAS No. 798576-99-5
  • Cat. No. CS-0539103
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₇NO₈
  • Molecular Weight 469.48
  • Synonym(s) FMOC aminotriacid
  • SMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CCC(=O)O)(CCC(=O)O)CCC(=O)O

Description

This fluorenylmethoxycarbonyl-protected amino acid derivative features a bifunctional side chain enabling dual conjugation. The C-terminal carboxyl group facilitates coupling reactions, while the N-terminal Fmoc moiety ensures stable protection during synthesis. Designed for efficient incorporation into peptide chains under standard conditions.

Application

4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-carboxyethyl)heptanedioic acid serves as a protected amino acid building block for the synthesis of peptide conjugates and complex heterocyclic scaffolds. The Fmoc group enables orthogonal deprotection under mild basic conditions, while the bis-carboxylic acid functionality supports efficient coupling reactions and metal chelation. Its bench-stable nature and compatibility with standard peptide synthesis workflows make it ideal for iterative solid-phase and solution-phase 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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

  • TPSA   150.23
  • LogP   3.8583
  • H_Acceptors   5
  • H_Donors   4
  • Rotatable_Bonds   12

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