Lawesson's reagent
| Names | |
|---|---|
| IUPAC name
2,4-Bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide | |
| Preferred IUPAC name
2,4-Bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-dithione | |
| Other names
Lawesson reagent; LR | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.038.944 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C14H14O2P2S4 | |
| Molar mass | 404.45 g·mol−1 |
| Appearance | Slightly yellow powder |
| Melting point | 228–231 °C (442–448 °F; 501–504 K) |
| Insoluble | |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H261, H302, H312, H332 | |
| P231+P232, P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P370+P378, P402+P404, P501 | |
| Related compounds | |
Related thiation agents |
Hydrogen sulfide, Phosphorus pentasulfide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Lawesson's reagent (LR) is a chemical compound used in organic synthesis as a thiation agent. Lawesson's reagent was first made popular by Sven-Olov Lawesson, who did not, however, invent it. Lawesson's reagent was first made in 1956 during a systematic study of the reactions of arenes with P4S10.