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CS-W001157 4
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Fmoc-N-Me-Asp(OMe)-OH

  • CAS No. 2044710-58-7

  • Cat. No. CS-0439302
  • Molecule weight383.39
  • Purity≥98%
  • MDL No.None

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

Fmoc-N-Me-Asp(OMe)-OH|CS-0439302

Structure of 2044710-58-7

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General Information

  • CAS No. 2044710-58-7
  • Cat. No. CS-0439302
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₂₁NO₆
  • Molecular Weight 383.39
  • Synonym(s) (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-methoxy-4-oxobutanoic acid
  • SMILES C(OC(N([C@@H](CC(OC)=O)C(O)=O)C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2

Description

Fmoc-N-Me-Asp(OMe)-OH is a protected aspartic acid derivative designed for efficient solid-phase peptide synthesis. The Fmoc group enables orthogonal deprotection, while the N-methyl and methyl ester functionalities enhance solubility and reduce racemization risk. This variant offers improved handling and incorporation fidelity in complex sequence assembly.

Application

Fmoc-N-Me-Asp(OMe)-OH serves as a valuable building block in peptide synthesis, offering enhanced stability and reduced racemization during coupling. The Fmoc group enables efficient orthogonal deprotection, while the N-methylated amine minimizes unwanted side reactions. The methyl ester facilitates straightforward conversion to carboxylic acid or amide derivatives, supporting versatile functionalization in solid-phase and solution-phase 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-P280-P302+P352

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Computational Chemistry Data

  • TPSA   93.14
  • LogP   2.8836
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   6

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