| Weight | 198.052 g/mol |
|---|---|
| Formula | C9H5Cl2N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4,7-Dichloroquinoline (86-98-6)
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- Regioselective Reactions of Organozinc Reagents with 2,4-Dichloroquinoline and 5,7-Dichloropyrazolo[1,5-a]pyrimidine (Journal of Organic Chemistry, 1999)
- 4-[(carboxymethyl)oxy]- and 4-[(carboxymethyl)amino]-5,7-dichloroquinoline-2-carboxylic acid : new antagonists of the strychnine-insensitive glycine binding site on the N-methyl-D-aspartate receptor complex (Journal of Medicinal Chemistry, 1990)
- The Role of Phenol in the Reaction of 4,7-Dichloroquinoline with Novol Diamine (Journal of the American Chemical Society, 1951)
- Synthesis of monoalkyl-substituted diamines and their condensation products with 4,7-dichloroquinoline. (Journal of the American Chemical Society, 1946)
- Reactions of heterocycles with thiophosgene. Part IV. ,4-Dichloro-2-isothiocyanatocinnamaldehyde, a product from 4,7-Dichloroquinoline (Journal of The Chemical Society-perkin Transactions 1, 1975)
- Comparison of the Suzuki cross-coupling reactions of 4,7-dichloroquinoline and 7-chloro-4-iodoquinoline with arylboronic acids using phosphine-free palladium catalysis in water (Canadian Journal of Chemistry, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CN=C2C=C1Cl)Cl
-
InChIKeyHXEWMTXDBOQQKO-UHFFFAOYSA-N
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