| Weight | 164.595 g/mol |
|---|---|
| Formula | C8H5ClN2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2-Chloroquinazoline (6141-13-5)
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- 2,4-diamino-5-chloroquinazoline analogues of trimetrexate and piritrexim : synthesis and antifolate activity (Journal of Medicinal Chemistry, 1994)
- 2-Chloroquinazoline: Synthesis and Reactivity of a Versatile Heterocyclic Building Block. (Tetrahedron Letters, 2006)
- 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)
- Synthesis and antileishmaniasis activity of 2-[2-chlorostyryl]-4-[-diethyl-amino--methylbutylamino]-7-chloroquinazoline diphosphate (Pharmaceutical Chemistry Journal, 1987)
- Expedient Synthesis of Quinazoline Analogues through Direct Nucleophilic Arylation/Alkylation of 2-Chloroquinazoline (Synthesis, 2016)
-
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
-
InChIKeyWMPTYRGXBUYONY-UHFFFAOYSA-N
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