Thermo Scientific Chemicals

9-Fluorenylmethyl chloroformate, 98+%, Thermo Scientific Chemicals

Catalog number: A11683.14
25 g, Each
Thermo Scientific Chemicals

9-Fluorenylmethyl chloroformate, 98+%, Thermo Scientific Chemicals

Catalog number: A11683.14
25 g, Each
Quantity
Catalog number: A11683.14
Price (USD)
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Chemical Identifiers

CAS
28920-43-6
IUPAC Name
(9H-fluoren-9-yl)methyl carbonochloridate
Molecular Formula
C15H11ClO2
InChI Key
IRXSLJNXXZKURP-UHFFFAOYSA-N
SMILES
ClC(=O)OCC1C2=CC=CC=C2C2=CC=CC=C12
Identification (FTIR)
Conforms
Appearance (Color)
White or cream or pale yellow
Assay (HPLC)
≥98.0%
Melting Point (clear melt)
60-64?C
Form
Powder

Description

Base sensitive amino protecting group for solid-phase peptide synthesis9-Fluorenylmethyl chloroformate is used in capillary electrophoresis. It acts as a reagent in the precolumn derivatization of amines for HPLC and fluorescent detection. Further, it is used for derivatizing amino acids for HPLC analysis. In addition to this, it is used to prepare N-Fmoc amino acids for solid-phase peptide synthesis and oligonucleotide synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Base sensitive amino protecting group for solid-phase peptide synthesis9-Fluorenylmethyl chloroformate is used in capillary electrophoresis. It acts as a reagent in the precolumn derivatization of amines for HPLC and fluorescent detection. Further, it is used for derivatizing amino acids for HPLC analysis. In addition to this, it is used to prepare N-Fmoc amino acids for solid-phase peptide synthesis and oligonucleotide synthesis.

Solubility
Soluble in dioxane.

Notes
Moisture sensitive. Store in a cool place. Incompatible with alcohols and amines.
RUO – Research Use Only

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