Weight | 129.55 g/mol |
---|---|
Formula | C4H4ClN3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2-Amino-4-chloropyrimidine (3993-78-0)
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- The structures of pyrimidines and purines. I. A determination of the structures of 2amino4methyl6chloropyrimidine and 2amino4,6dichloropyrimidine by Xray methods (Acta Crystallographica, 1948)
- Synthesis and biological study of 2-amino-4-aryl-5-chloropyrimidine analogues as inhibitors of VEGFR-2 and cyclin dependent kinase 1 (CDK1). (Bioorganic & Medicinal Chemistry Letters, 2007)
- Electrolytic Reduction of 2Amino4chloropyrimidine, 2Amino4choro6methylpyrimidine, and 2Aminopyrimidine (Journal of The Electrochemical Society, 1957)
- Reaction of 2,2'-anhydro-1-(-D-arabinofuranosyl)-6-azauracil, 4-chloropyrimidine and 6-chloropurine nucleosides with amino acids (Collection of Czechoslovak Chemical Communications, 1984)
- Raman and infrared spectra, normal coordinate analysis and ab initio calculations of 4-Amino-2-chloropyrimidine-5-carbonitrile (Journal of Molecular Structure, 2016)
- Dehalogenation of 2-Amino-4-methyl-6-chloropyrimidine (Journal of the American Chemical Society, 1951)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(N=C1Cl)N
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InChIKeyDBGFGNCFYUNXLD-UHFFFAOYSA-N
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