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9-Fluorenylmethyl chloroformate, 98+%, Thermo Scientific Chemicals
Store cold
$45.56 - $606.71
Chemical Identifiers
| CAS | 28920-43-6 |
|---|---|
| Molecular Formula | C15H11ClO2 |
| Molecular Weight (g/mol) | 258.701 |
| MDL Number | MFCD00001138 |
| InChI Key | IRXSLJNXXZKURP-UHFFFAOYSA-N |
| Synonym | 9-fluorenylmethyl chloroformate, fmoc-cl, fmoc-chloride, fmoc chloride, 9h-fluoren-9-ylmethyl chloroformate, carbonochloridic acid, 9h-fluoren-9-ylmethyl ester, 9-fluorenylmethoxycarbonyl chloride, 9-fluorenylmethylchloroformate, 9h-fluoren-9-yl methyl carbonochloridate, 9h-fluoren-9-ylmethoxy carbonyl chloride |
| PubChem CID | 34367 |
| IUPAC Name | 9H-fluoren-9-ylmethyl carbonochloridate |
| SMILES | C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1168303
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Thermo Scientific Chemicals
A1168303 |
1 g |
Each for $45.56
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AAA1168306
|
Thermo Scientific Chemicals
A1168306 |
5 g |
Each for $139.23
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AAA1168314
|
Thermo Scientific Chemicals
A1168314 |
25 g |
Each for $606.71
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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.
ApplicationsBase 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.
Chemical Identifiers
| 28920-43-6 | |
| 258.701 | |
| IRXSLJNXXZKURP-UHFFFAOYSA-N | |
| 34367 | |
| C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl |
| C15H11ClO2 | |
| MFCD00001138 | |
| 9-fluorenylmethyl chloroformate, fmoc-cl, fmoc-chloride, fmoc chloride, 9h-fluoren-9-ylmethyl chloroformate, carbonochloridic acid, 9h-fluoren-9-ylmethyl ester, 9-fluorenylmethoxycarbonyl chloride, 9-fluorenylmethylchloroformate, 9h-fluoren-9-yl methyl carbonochloridate, 9h-fluoren-9-ylmethoxy carbonyl chloride | |
| 9H-fluoren-9-ylmethyl carbonochloridate |
Specifications
| 28920-43-6 | |
| 98% | |
| MFCD00001138 | |
| UN2923 | |
| Moisture sensitive | |
| Soluble in dioxane. | |
| C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl | |
| 258.701 | |
| 258.7 | |
| 9-Fluorenylmethyl chloroformate |
| 60°C to 64°C | |
| C15H11ClO2 | |
| 1 g | |
| 2279177 | |
| 9-fluorenylmethyl chloroformate, fmoc-cl, fmoc-chloride, fmoc chloride, 9h-fluoren-9-ylmethyl chloroformate, carbonochloridic acid, 9h-fluoren-9-ylmethyl ester, 9-fluorenylmethoxycarbonyl chloride, 9-fluorenylmethylchloroformate, 9h-fluoren-9-yl methyl carbonochloridate, 9h-fluoren-9-ylmethoxy carbonyl chloride | |
| IRXSLJNXXZKURP-UHFFFAOYSA-N | |
| 9H-fluoren-9-ylmethyl carbonochloridate | |
| 34367 | |
| 98% |
Safety and Handling
GHS H Statement
H314-H318-H302-H332
P260-P264b-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P501c
H302+H312+H332-H314-H335
DOTInformation : Hazard Class: 6.1; Packaging Group: II
EINECSNumber : 249-313-6
RTECSNumber : LQ6250000
TSCA : No
storageNote1 : Moisture Sensitive
Recommended Storage : Keep cold; Store under Nitrogen
RUO – Research Use Only