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CS-W001157 4
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N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-ethyl-N-methyl-L-serine

  • CAS No. 1931107-98-0

  • Cat. No. CS-0096678
  • Purity≥97%
  • MDL No.None

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

N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-ethyl-N-methyl-L-serine|CS-0096678

Structure of 1931107-98-0

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General Information

  • CAS No. 1931107-98-0
  • Cat. No. CS-0096678
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₂₃NO₅
  • Molecular Weight 369.41
  • Synonym(s) None
  • SMILES O=C(O)[C@H](COCC)N(C(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)C

Description

This fluorenylmethoxycarbonyl-protected serine derivative features a stable, electron-rich fluoren-9-ylmethoxy carbonyl group that enables efficient coupling in peptide synthesis. The O-ethyl and N-methyl substitutions enhance solubility and reduce side reactions, while the protected hydroxyl and amino groups provide orthogonal functionality for sequential derivatization.

Application

N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-ethyl-N-methyl-L-serine serves as a versatile, bench-stable amino acid derivative for solid-phase peptide synthesis. Its Fmoc group enables orthogonal protection, while the O-ethyl and N-methyl functionalities provide enhanced solubility and reduced racemization risk during coupling. The molecule facilitates efficient incorporation of modified serine residues into peptide sequences, supporting both manual and automated synthesis workflows with high fidelity and ease of purification.

Safety Information

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GHS Pictogram : N/A
GHS No : N/A
Signal Word : N/A
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

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Computational Chemistry Data

  • TPSA   76.07
  • LogP   3.357
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   7

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