266318-79-0

Basic information

• Product Name: FMOC-D--LEU-OH
• Synonyms: (s)-3-(fmoc-amino)-4-methylpentanoic acid;(S)-3-(Fmoc-amino)-4-methylpentanoic acid, Fmoc-D-β-Homoval-OH;Fmoc-D-β-Homoval-OH;(3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-methylpentanoic acid;(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanoic acid;Fmoc-s-β-homovaline;(9H-Fluoren-9-yl)MethOxy]Carbonyl D-β-homovaline
• CAS NO: 266318-79-0
• Molecular Formula: C₂₁H₂₃NO₄
• Molecular Weight: 353.41
• Mol File: 266318-79-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 563.9±33.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.41±0.10(Predicted)
• CAS DataBase Reference: FMOC-D--LEU-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-D--LEU-OH(266318-79-0)
• EPA Substance Registry System: FMOC-D--LEU-OH(266318-79-0)

Safety Data

• WGK Germany: 3
• F: 10
• Hazardous Substances Data: 266318-79-0(Hazardous Substances Data)

Usage

General Description

FMOC-D-LEU-OH, also known as N-(9-fluorenylmethoxycarbonyl)-D-leucine, is a synthetic compound used in organic chemistry and biochemistry. It is a derivative of the amino acid leucine, and its structure includes a fluorenylmethoxycarbonyl (FMOC) protecting group attached to the amino group of the leucine molecule. FMOC-D--LEU-OH is often used in the solid-phase peptide synthesis as a building block for creating peptide chains. FMOC-D-LEU-OH is commonly used in research and drug development as a key component in the production of peptide-based drugs and biomolecules. Its specific structure and properties make it valuable for the study and manipulation of peptide molecules in a laboratory setting.

Relevant articles and documents

Fibrinogen receptor antagonist and pharmaceutical compositions comprising the same

Compounds of the following general formula (I) and pharmaceutically acceptable salts thereof.