2-Vinyl-4,6-diamino-1,3,5-triazine

2-Vinyl-4,6-diamino-1,3,5-triazine
Names
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)
ChemSpider
ECHA InfoCard 100.102.330 Edit this at Wikidata
EC Number
  • 424-800-8
  • InChI=1S/C5H7N5/c1-2-3-8-4(6)10-5(7)9-3/h2H,1H2,(H4,6,7,8,9,10)
    Key: ZXLYUNPVVODNRE-UHFFFAOYSA-N
  • C=CC1=NC(=NC(=N1)N)N
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).

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

  1. ^ 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.
  2. ^ 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.