| Weight | 229.458 g/mol |
|---|---|
| Formula | C3H3Cl3N6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
TRICHLOROMELAMINE (7673-09-8, 12379-38-3)
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- Selective oxidation of alcohols and oxidative lactonization of diols with trichloromelamine (Journal of Organic Chemistry, 1993)
- 1,3-Dichloro-5,5-dimethylhydantoin (DCH) and Trichloromelamine (TCM) as Efficient Catalysts for the Chemoselective Trimethylsilylation of Hydroxyl Group with 1,1,1,3,3,3-Hexamethyldisilazane (HMDS) under Mild Conditions (Journal of The Chinese Chemical Society, 2009)
- One-pot synthesis of 2,4,5-tri-substituted-1H-imidazoles promoted by trichloromelamine (Current Chemistry Letters, 2013)
- Efficient procedure for chemoselective N-nitrosation of secondary amines with trichloromelamine-NaNO2 (Russian Journal of Organic Chemistry, 2007)
- Simple, Convenient and Heterogeneous Method for Conversion of Urazoles to Triazolinediones Using N,N,N,NTetrabromobenzene1,3disulfonylamide or Trichloromelamine under Mild and Heterogeneous Conditions. (Synthesis, 2006)
- Synergistic Effect Between Sb2O3 NanoparticlesTrichloromelamine and Carbon Nanotube on the Flame Retardancy and Thermal Stability of the Cellulose Acetate (Journal of Cluster Science, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1(=NC(=NC(=N1)NCl)NCl)NCl
-
InChIKeyKEPNSIARSTUPGS-UHFFFAOYSA-N
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