Cellocidin
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| Names | |
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| Preferred IUPAC name
But-2-ynediamide | |
| Other names
Cellocidin; Lenamycin; Acetylene diamide; Acetylenedicarboxamide; Acetylenedicarboxylic acid diamide
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
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| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
| MeSH | C015739 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C4H4N2O2 | |
| Molar mass | 112.088 g·mol−1 |
| Density | 1.411 g/mL |
| Melting point | 179 °C (354 °F; 452 K) |
| log P | −1.2 |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Skin irritant; may cause respiratory tract irritation |
| GHS labelling: | |
| Warning | |
| H302 | |
| P264, P270, P301+P312, P330, P501 | |
| Flash point | 216 °C (421 °F; 489 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cellocidin (2-butynediamide) is an organic chemical compound with the molecular formula C4H4O2N2. This compound was isolated from Streptomyces chibaensis, Streptomyces reticuli and Streptomyces sp. SF-536.
Structure
[edit | edit source]Cellocidin is an organic compound containing 4 carbon atoms, 4 hydrogen atoms, 2 oxygen atoms, and 2 nitrogen atoms. It contains one carbon-carbon triple bond between carbons 2 and 3, and two carbon-oxygen double bonds off carbon 1 and carbon 4. Cellocidin contains two identical amide groups connected together by the central carbons (carbons 2 and 3).
References
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