194718-17-7

Basic information

• Product Name: FMOC-L-HOLYS(BOC)-OH
• Synonyms: FMOC-L-HLYS(BOC);FMOC-L-HOLYS(BOC)-OH;FMOC-D, L-HLYS(BOC);N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ZETA-T-BUTYLOXYCARBONYL-L-HOMOLYSINE;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ZETA-TERT-BUTYLOXYCARBONYL-HOMO-L-LYSINE;N-ALPHA-(9-FLUOROENYLMETHYLOXYCARBONYL)-N-ZETA-T-BUTYLOXYCARBONYL-L-HOMOLYSINE;(S)-FMoc-2-aMino-7-(Boc-aMino)-heptanoic acid;(9H-Fluoren-9-yl)MethOxy]Carbonyl L-HomoLysine(Boc)-OH
• CAS NO: 194718-17-7
• Molecular Formula: C27H34N2O6
• Molecular Weight: 482.57
• Mol File: 194718-17-7.mol

Chemical Properties

• Boiling Point: 692.7±55.0 °C(Predicted)
• Appearance: /
• Density: 1.195±0.06 g/cm3(Predicted)
• PKA: 3.90±0.21(Predicted)
• CAS DataBase Reference: FMOC-L-HOLYS(BOC)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-L-HOLYS(BOC)-OH(194718-17-7)
• EPA Substance Registry System: FMOC-L-HOLYS(BOC)-OH(194718-17-7)

Safety Data

• Hazardous Substances Data: 194718-17-7(Hazardous Substances Data)

Usage

Uses

Used in Organic Chemistry:
FMOC-L-HOLYS(BOC)-OH is used as a building block in peptide synthesis for the creation of longer peptide chains. Its role is crucial in solid-phase peptide synthesis, where the FMOC and BOC protecting groups are selectively removed to facilitate the addition of other amino acids, thus extending the peptide chain.
Used in Pharmaceutical Development:
In the pharmaceutical industry, FMOC-L-HOLYS(BOC)-OH is utilized as a reagent in the preparation of peptide-based drugs. Its protective groups ensure that the peptide synthesis process can be controlled and specific, which is essential for the development of targeted and effective therapeutics.
Used in Research:
FMOC-L-HOLYS(BOC)-OH also serves as a valuable research tool in the study of protein-protein interactions. By incorporating this compound into peptides, researchers can investigate and understand the mechanisms of these interactions, which is fundamental for advancing knowledge in biochemistry and molecular biology.