Fluorenylmethyloxycarbonyl chloride
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| Names | |
|---|---|
| Preferred IUPAC name (9H-Fluoren-9-yl)methyl carbonochloridate | |
| Other names 9-Fluorenylmethyl chloroformate; 9-Fluorenylmethoxycarbonyl chloride; Fmoc-chloride | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.044.816 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C15H11ClO2 | |
| Molar mass | 258.70 g·mol−1 | 
| Melting point | 62 to 64 °C (144 to 147 °F; 335 to 337 K) | 
| Hazards | |
| GHS labelling: | |
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| Danger | |
| H314 | |
| P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P330, P363, P405, P501 | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Fluorenylmethyloxycarbonyl chloride (Fmoc-Cl) is a chloroformate ester. It is used to introduce the fluorenylmethyloxycarbonyl protecting group as the Fmoc carbamate.
Preparation
This compound may be prepared by reacting 9-fluorenylmethanol with phosgene:[2]
References
- ^ Fmoc chloride at Sigma-Aldrich
- ^ Carpino, Louis A.; Han, Grace Y. (1972). "9-Fluorenylmethoxycarbonyl amino-protecting group". The Journal of Organic Chemistry. 37 (22): 3404. doi:10.1021/jo00795a005.


