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1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclobutane-1-carboxylic acid

  • CAS No. 885951-77-9

  • Cat. No. CS-0130262
  • Purity≥98%
  • MDL No.MFCD02682624

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

1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclobutane-1-carboxylic acid|CS-0130262

Structure of 885951-77-9

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General Information

  • CAS No. 885951-77-9
  • Cat. No. CS-0130262
  • Purity ≥98%
  • MDL No. MFCD02682624
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₀H₁₉NO₄
  • Molecular Weight 337.37
  • Synonym(s) 1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclobutanecarboxylic acid
  • SMILES O=C(C1(NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)CCC1)O

Description

This fluorenylmethoxycarbonyl-protected cyclobutane derivative serves as a robust, bench-stable amino acid surrogate for peptide synthesis. The rigid cyclobutane scaffold imparts conformational constraint, while the Fmoc group enables orthogonal deprotection. Ideal for incorporating sterically defined residues into bioactive peptides and cyclic architectures.

Application

1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclobutane-1-carboxylic acid serves as a robust, bench-stable amino acid derivative for peptide synthesis. The Fmoc group enables efficient N-terminal protection with orthogonal deprotection under mild basic conditions. The cyclobutane core provides conformational rigidity, facilitating the incorporation of constrained motifs in bioactive peptide sequences. Compatible with standard coupling protocols and offering clean purification via crystallization or chromatography, this building block supports scalable synthesis of cyclic peptides and peptidomimetics.

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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   3.5324
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   4

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