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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxyphenyl)propanoic acid

  • CAS No. 501015-30-1

  • Cat. No. CS-0181517
  • Purity≥97%
  • MDL No.MFCD03427976

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

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxyphenyl)propanoic acid|CS-0181517

Structure of 501015-30-1

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General Information

  • CAS No. 501015-30-1
  • Cat. No. CS-0181517
  • Purity ≥97%
  • MDL No. MFCD03427976
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₃NO₅
  • Molecular Weight 417.45
  • Synonym(s) Fmoc-beta-(S)-4-methoxyphenylalanine
  • SMILES OC(C[C@@H](C1=CC=C(C=C1)OC)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)=O

Description

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxyphenyl)propanoic acid features a chiral center flanked by a fluorenylmethyl carbamate protecting group and a para-methoxyphenyl moiety, enabling direct incorporation into peptide synthesis workflows. This bench-stable derivative supports efficient N-terminal protection with orthogonal deprotection compatibility.

Application

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxyphenyl)propanoic acid serves as a robust chiral building block for peptide synthesis and medicinal chemistry applications. The Fmoc group enables efficient N-terminal protection with orthogonal deprotection under mild basic conditions, while the pendant 4-methoxyphenyl moiety provides structural rigidity and enhanced solubility. Its bench-stable nature and compatibility with standard coupling protocols facilitate reliable use in solid-phase and solution-phase syntheses.

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-H312-H332
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501

Quality Control

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Computational Chemistry Data

  • TPSA   84.86
  • LogP   4.7497
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   7

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