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CS-W001157 4
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Fmoc-(R)-3-Amino-4-(4-chloro-phenyl)-butyric acid

  • CAS No. 331763-60-1

  • Cat. No. CS-0061680
  • Purity≥97%
  • MDL No.None

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

Fmoc-(R)-3-Amino-4-(4-chloro-phenyl)-butyric acid|CS-0061680

Structure of 331763-60-1

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General Information

  • CAS No. 331763-60-1
  • Cat. No. CS-0061680
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₂ClNO₄
  • Molecular Weight 435.90
  • Synonym(s) (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-chlorophenyl)butanoic acid
  • SMILES ClC=1C=CC(=CC1)C[C@H](CC(O)=O)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O

Description

Fmoc-(R)-3-Amino-4-(4-chlorophenyl)butyric acid is a chiral building block featuring a fluorinated benzyl side chain and a protected α-amino group. This derivative enables efficient incorporation into peptide sequences via solid-phase synthesis, offering enhanced solubility and stability under standard conditions. The para-chlorophenyl moiety provides steric and electronic modulation for tailored molecular design.

Application

Fmoc-(R)-3-Amino-4-(4-chlorophenyl)butyric acid serves as a versatile building block for the synthesis of peptide-based pharmaceuticals and bioactive heterocycles. Its well-defined stereochemistry and robust Fmoc protection enable efficient solid-phase peptide synthesis, while the pendant 4-chlorophenyl group provides a handle for downstream functionalization via cross-coupling reactions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it ideal for high-throughput medicinal chemistry campaigns.

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-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   5.2645
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   7

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