| Weight | 148.98 g/mol |
|---|---|
| Formula | C4H2Cl2N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3,6-Dichloropyridazine (141-30-0)
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- Synthesis in the Pyridazine Series. I. Pyridazine and 3,6-Dichloropyridazine (Journal of the American Chemical Society, 1951)
- Properties of the shortlived triplet states of pyridazine and 3,6dichloropyridazine studied by a timeresolved EPR method (Journal of Chemical Physics, 1986)
- Molecular Structure of Gaseous Pyridazine and 3,6-Dichloropyridazine by Electron Diffraction. (Acta Chemica Scandinavica, 1977)
- Highly selective mono-substitution in Pd-catalyzed cross-coupling reactions of 3,6-dichloropyridazine with organozinc compounds (Tetrahedron Letters, 2005)
- Radical Mediated CH Functionalization of 3,6-Dichloropyridazine: Efficient Access to Novel Tetrahydropyridopyridazines (Organic Letters, 2015)
- Synthesis of highly refractive and transparent poly(arylene sulfide sulfone) based on 4,6-dichloropyrimidine and 3,6-dichloropyridazine (Polymer, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 -
SMILESC1=CC(=NN=C1Cl)Cl
-
InChIKeyGUSWJGOYDXFJSI-UHFFFAOYSA-N
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