Weight | 183.425 g/mol |
---|---|
Formula | C4HCl3N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
3,4,5-Trichloropyridazine (14161-11-6)
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- Experimental and Theoretical Analysis of the Vibrational Spectra and Theoretical Study of the Structures of 3,6-Dichloropyridazine and 3,4,5-Trichloropyridazine (Journal of Physical Chemistry A, 2000)
- Chemistry of the phenoxathiins and isosterically related heterocycles. XIX.. The crystal and molecular structure of 1-N,N-dimethylamino-2,3-diazaphenoxathiin: An interesting product isolated from the reaction of o-mercaptophenol with 3,4,5-trichloropyridazine in N,N-dimethylformamide (Journal of Heterocyclic Chemistry, 1981)
- A novel synthesis of 3, 4, 5-trichloropyridazine (Journal of Heterocyclic Chemistry, 1967)
- Primary irritant effect of 3,4,5trichloropyridazine (Contact Dermatitis, 1988)
- Experimental contact sensitization with 3,4,5trichloropyridazine (Contact Dermatitis, 1988)
- ChemInform Abstract: Studies on Syntheses and Reactions of Methoxypyridazines. Part 1. Methoxylation of 3,4,5-Trichloropyridazine. (ChemInform, 1987)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C(=C(N=N1)Cl)Cl)Cl
-
InChIKeyGBAOOJAWDCNOGO-UHFFFAOYSA-N
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