Description
Fmoc chloride 97%, 5G
Synonym: 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate, Fmoc-Cl
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CAS Number 28920-43-6
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Empirical Formula (Hill Notation) C15H11ClO2
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Molecular Weight 258.70
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Beilstein/REAXYS Number 2279177
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EC Number 249-313-6
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MDL number MFCD00001138
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PubChem Substance ID 24849875
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NACRES NA.22
Properties
Related Categories | Amine Protection, Chemical Biology, Chemical Synthesis, Other Protecting and Derivatizing Reagents, Peptide Synthesis and Peptide Chemistry,
Protecting and Derivatizing Reagents, Protection and Derivatization, Synthetic Reagents
Less... |
assay | 97% |
application(s) | peptide synthesis: suitable |
mp | 62-64 °C (lit.) |
functional group | Fmoc |
storage temp. | 2-8°C |
SMILES string | ClC(=O)OCC1c2ccccc2-c3ccccc13 |
InChI | 1S/C15H11ClO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2 |
InChI key | IRXSLJNXXZKURP-UHFFFAOYSA-N |
Packaging
1, 5, 25 g in glass bottle
Application
Amino acid derivatizing agent for HPLC analysis.[1] N-protecting reagent for peptide[2] and oligonucleotide[3] syntheses.
Reagent for amino group protection recently used in the synthesis of a bicyclic proline analog.[4]
Reagent for derivatizing amino acids for HPLC amino acid analysis and for preparing N-Fmoc amino acids for solid-phase peptide synthesis.