''cis''-Butene-1,4-diol
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| Identifiers | |
|---|---|
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.025.532 |
| EC Number | 228-085-1 |
PubChem CID |
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| UNII | |
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| Properties | |
| C4H8O2 | |
| Molar mass | 88.11 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 pictograms |  |
| GHS signal word | Warning |
| H302, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313, P362, P403+233, 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 react 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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