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CS-W001157 4
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Boc-R-3-amino-4-(4-tert-butylphenyl)-butyric acid

  • CAS No. 401916-48-1

  • Cat. No. CS-0182733
  • Purity≥97%
  • MDL No.MFCD03093578

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

Boc-R-3-amino-4-(4-tert-butylphenyl)-butyric acid|CS-0182733

Structure of 401916-48-1

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General Information

  • CAS No. 401916-48-1
  • Cat. No. CS-0182733
  • Purity ≥97%
  • MDL No. MFCD03093578
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₂₉NO₄
  • Molecular Weight 335.44
  • Synonym(s) Boc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid
  • SMILES CC(C)(C1=CC=C(C=C1)C[C@H](CC(O)=O)NC(OC(C)(C)C)=O)C

Description

Boc-R-3-amino-4-(4-tert-butylphenyl)-butyric acid is a sterically hindered, bench-stable amino acid derivative featuring a bulky tert-butyl group that enhances solubility and minimizes side reactions. This protected building block integrates efficiently into peptide synthesis workflows, offering reliable coupling and stability under standard conditions.

Application

Boc-R-3-amino-4-(4-tert-butylphenyl)-butyric acid serves as a versatile chiral building block for the synthesis of bioactive molecules, particularly in peptide and medicinal chemistry. The Boc-protected amine enables straightforward N-terminal functionalization, while the pendant tert-butylphenyl group provides steric bulk and metabolic stability. Its well-defined stereochemistry and bench-stable nature facilitate reliable coupling reactions and purification, making it ideal for constructing complex scaffolds in API development 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   75.63
  • LogP   3.8946
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   5

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