|  | |
| Names | |
|---|---|
| Preferred IUPAC name (2Z)-But-2-ene-1,4-diol | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.025.532 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| 
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| 
 | |
| Properties | |
| C4H8O2 | |
| Molar mass | 88.106 g·mol−1 | 
| Density | 1.07 | 
| Melting point | 7 °C (45 °F; 280 K) | 
| Boiling point | 141–149 °C (286–300 °F; 414–422 K) | 
| very soluble | |
| Solubility | ethanol, acetone | 
| Hazards | |
| GHS labelling: | |
|  | |
| Warning | |
| H302, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
| Flash point | 128 °C (262 °F; 401 K) | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
cis-Butene-1,4-diol is a chemical compound used in the production of endosulfan. It reacts with hexachlorocyclopentadiene to form endosulfan diol. Endosulfan diol then reacts with thionyl chloride to form endosulfan.[1]
References
- ↑ "Endosulfan - Molecule of the Month June 2011 - HTML-only version". Molecule of the Month.
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