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Fmoc-Gly-NH-CH2-O-CH2COOH

  • CAS No. 1599440-08-0

  • Cat. No. CS-0064391
  • Molecule weight384.38
  • Purity≥95%
  • MDL No.MFCD32639967

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

Fmoc-Gly-NH-CH2-O-CH2COOH|CS-0064391

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General Information

  • CAS No. 1599440-08-0
  • Cat. No. CS-0064391
  • Purity ≥95%
  • MDL No. MFCD32639967
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₀H₂₀N₂O₆
  • Molecular Weight 384.38
  • Synonym(s) 1-(9H-Fluoren-9-yl)-3,6-dioxo-2,9-dioxa-4,7-diazaundecan-11-oic acid
  • SMILES O=C(O)COCNC(CNC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)=O

Description

Fmoc-Gly-NH-CH2-O-CH2COOH is a specialized amino acid derivative designed for peptide synthesis and conjugation workflows. The Fmoc group enables efficient N-terminal protection, while the hydrophilic linker facilitates solubility and selective coupling. This compound integrates seamlessly into solid-phase protocols, offering reliable deprotection and minimal side reactions under standard conditions.

Application

Fmoc-Gly-NH-CH₂-O-CH₂COOH serves as a versatile bifunctional building block for peptide and peptidomimetic synthesis, enabling efficient conjugation via its terminal carboxylic acid and amine-functionalized linker. The Fmoc group provides orthogonal protection for the amino terminus, while the glycinyl spacer offers enhanced solubility and stability. Its robust compatibility with standard coupling reagents and ease of purification make it well-suited for solid-phase and solution-phase workflows in medicinal chemistry and macrocycle construction.

Safety Information

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Computational Chemistry Data

  • TPSA   113.96
  • LogP   1.7
  • H_Acceptors   5
  • H_Donors   3
  • Rotatable_Bonds   8

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