| Weight | 183.425 g/mol |
|---|---|
| Formula | C4HCl3N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,4,6-Trichloropyrimidine (3764-01-0)
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- 2,4,6-TRICHLOROPYRIMIDINE. REACTION WITH 4-SUBSTITUTED PHENOLATE IONS (Journal of Heterocyclic Chemistry, 1998)
- 2,4,6-TRICHLOROPYRIMIDINE. REACTION WITH ETHANOLAMINE AND DIETHANOLAMINE (Journal of Heterocyclic Chemistry, 1995)
- Efficient and regioselective 4-amino-de-chlorination of 2,4,6-trichloropyrimidine with N-sodium carbamates (Tetrahedron Letters, 2000)
- 2,4,6-trichloropyrimidine. Reaction with anilines (Journal of Heterocyclic Chemistry, 2000)
- 2,4,6-TRICHLOROPYRIMIDINE. REACTION WITH SODIUM AMIDE (Journal of Heterocyclic Chemistry, 1999)
- Regioselective solid-phase 4-amino-de-chlorination of 2,4,6-trichloropyrimidine by resin-supported N-potassium carbamates (Tetrahedron Letters, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(N=C(N=C1Cl)Cl)Cl
-
InChIKeyDPVIABCMTHHTGB-UHFFFAOYSA-N
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