// Workers AI · dad joke modeWhy was 2-Vinyl-4,6-diamino-1,3,5-triazine a great singer? It had a tri-azine voice.
(Redirected from Vinyl triazine)
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| Names | |
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| Preferred IUPAC name
6-Ethenyl-1,3,5-triazine-2,4-diamine | |
| Other names
2,4-diamino-6-vinyl-s-triazine, 2-vinyl-4,6-diamino-1,3,5-triazine, VDT | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.102.330 |
| EC Number |
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PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| C5H7N5 | |
| Molar mass | 137.146 g·mol−1 |
| Appearance | white solid |
| Melting point | 239–241 °C (462–466 °F; 512–514 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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2-Vinyl-4,6-diamino-1,3,5-triazine is an organic compound with the formula (H2NC)2N3CCH=CH2. The molecule consists of a vinyl group (-CH=CH2) attached to a 2,4-diaminotriazine. A colorless solid, it is a monomeric precursor to polymers with hydrogen-bonding substituents.[1][2]
References
[edit]- ↑ Ilhan, Faysal; Gray, Mark; Rotello, Vincent M. (2001). "Reversible Side Chain Modification through Noncovalent Interactions. "Plug and Play" Polymers". Macromolecules. 34 (8): 2597–2601. Bibcode:2001MaMol..34.2597I. doi:10.1021/ma001700r.
- ↑ Xie, Xun; Huang, Lei; Liu, Zuifang; Xie, Weihong; Wang, Xiatao (2019). "Synthesis of poly(2-vinyl-4,6-diamino-1,3,5-triazine) nanoparticles by semi-continuous precipitation polymerization, characterization and application to bovine hemoglobin adsorption". Reactive and Functional Polymers. 141: 58–67. doi:10.1016/j.reactfunctpolym.2019.01.004. S2CID 155724431.