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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(3-fluorophenyl)propanoic acid

  • CAS No. 1820567-10-9

  • Cat. No. CS-0179541
  • Purity≥97%
  • MDL No.None

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

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(3-fluorophenyl)propanoic acid|CS-0179541

Structure of 1820567-10-9

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General Information

  • CAS No. 1820567-10-9
  • Cat. No. CS-0179541
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₂FNO₄
  • Molecular Weight 419.44
  • Synonym(s) None
  • SMILES O=C(O)[C@H](CC1=CC=CC(F)=C1)N(C(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C

Description

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(3-fluorophenyl)propanoic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected amine and a sterically defined β-amino acid scaffold. This configuration enables efficient incorporation into peptide sequences, where the Fmoc group facilitates orthogonal protection during solid-phase synthesis. The para-fluorinated aryl moiety enhances solubility and modulates electronic properties in synthetic intermediates.

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(3-fluorophenyl)propanoic acid serves as a valuable chiral building block for peptide synthesis, enabling efficient incorporation of sterically demanding, fluorinated aromatic side chains. The Fmoc group provides orthogonal protection with excellent bench stability and compatibility with standard coupling protocols. The methylamino functionality offers tunable basicity and enhanced solubility, facilitating purification and reaction scalability 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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

  • TPSA   66.84
  • LogP   4.7023
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   6

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