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CS-W001157 4
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-chlorophenyl)propanoic acid

  • CAS No. 511272-53-0

  • Cat. No. CS-0062191
  • Purity≥97%
  • MDL No.None

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

(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-chlorophenyl)propanoic acid|CS-0062191

Structure of 511272-53-0

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General Information

  • CAS No. 511272-53-0
  • Cat. No. CS-0062191
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₄H₂₀ClNO₄
  • Molecular Weight 421.87
  • Synonym(s) Fmoc-R-3-Amino-3-(3-chloro-phenyl)-propionic acid
  • SMILES O=C(O)C[C@H](C1=CC(Cl)=CC=C1)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O

Description

Fmoc-(R)-3-Amino-3-(3-chlorophenyl)-propionic acid is a bench-stable, moisture-tolerant building block for peptide synthesis. This chiral amino acid features a para-chlorinated aromatic side chain that enhances lipophilicity and metabolic stability. The Fmoc group enables efficient N-terminal protection during solid-phase peptide coupling workflows.

Application

Fmoc-(R)-3-Amino-3-(3-chlorophenyl)-propionic acid serves as a valuable building block for the synthesis of peptidomimetics and bioactive scaffolds. Its Fmoc-protected amine enables efficient solid-phase peptide synthesis, while the pendant 3-chlorophenyl group provides steric and electronic modulation. The molecule exhibits excellent bench stability, facilitates straightforward purification, and tolerates a broad range of reaction conditions, making it ideal for iterative coupling and heterocycle formation 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   5.3945
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

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