| Weight | 164.595 g/mol |
|---|---|
| Formula | C8H5ClN2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Chloroquinazoline (5190-68-1)
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- 2,4-diamino-5-chloroquinazoline analogues of trimetrexate and piritrexim : synthesis and antifolate activity (Journal of Medicinal Chemistry, 1994)
- Quinazoline derivatives; the synthesis of 4-(3'-diethylaminopropoxy)-6-chloroquinazoline (SN 12,254). (Journal of the American Chemical Society, 1946)
- 4-(4'-diethylamino-l'-methylbutylamino)-7-chloroquinazoline. (Journal of the American Chemical Society, 1946)
- The reaction of 4-chloroquinazoline with lithium piperidide in piperidine and potassium amide in liquid ammonia at 75 (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- Formation Mechanism of 2-(N-Alkyl-4-chlorobutylamino)-4-chloroquinazoline (Heterocycles, 1982)
- Ring opening of 4-chloroquinazoline into 2-arylmethyleneaminobenzonitrile by Grignard reaction (Heterocycles, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=NC=N2)Cl
-
InChIKeyGVRRXASZZAKBMN-UHFFFAOYSA-N
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Similar Compounds
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quinazolin-8-ol
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7-chloroquinazoline-2,4(1h,3h)-dione
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4-Chloro-6-methoxy-2-methylquinoline
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2,7-Dichloro-4-methylquinoline
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1 alternate name
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4-chloro-2,6-dimethylquinoline
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4-Chloroquinazoline
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