| Weight | 95.105 g/mol |
|---|---|
| Formula | C4H5N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
4-Aminopyrimidine (591-54-8)
Score:
#6249 in Chemistry
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- Nitrogen Base Adducts with Silver(I)p-Toluenesulfonate: Syntheses and Single Crystal X-ray Characterizations of the Adducts with Pyridine (1:1), 2-Aminopyridine (1:2), 2-Aminopyrimidine (1:1), 4,6-Dimethyl-2-aminopyrimidine (2:3), and 3-Aminobenzoic Acid (1:2) and the Crystal Structure of the Parent Silver(I)p-Toluenesulfonate (Inorganic Chemistry, 1998)
- Synthesis, spectroscopic and biological studies on the new symmetric Schiff base derived from 2,6-diformyl-4-methylphenol with N-aminopyrimidine. (European Journal of Medicinal Chemistry, 2010)
- 2Aminopyrimidine4,6diol as an Efficient Ligand for SolventFree CopperCatalyzed NArylations of Imidazoles with Aryl and Heteroaryl Halides (Journal of Organic Chemistry, 2006)
- Regiocontrolled GoldCatalyzed [2+2+2] Cycloadditions of Ynamides with Two Discrete Nitriles to Construct 4Aminopyrimidine Cores (Angewandte Chemie, 2014)
- Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2 (Bioorganic & Medicinal Chemistry Letters, 2003)
- Matrix-isolation FT-IR studies and ab-initio calculations of hydrogen-bonded complexes of molecules modeling cytosine or isocytosine tautomers. 2. 4-Aminopyridine and 4-aminopyrimidine complexes with H2O in Ar matrices (The Journal of Physical Chemistry, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=CN=C1N
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InChIKeyOYRRZWATULMEPF-UHFFFAOYSA-N
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Similar Compounds
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cytosine
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4-Amino-6-methoxypyrimidine
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2-(trifluoromethyl)pyrimidine-4,6-diamine
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4-Chloro-6-hydrazinopyrimidine
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6-Chloro-N-methylpyrimidin-4-amine
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461-98-3
(461-98-3)
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1749-68-4
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4316-98-7
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[(4,6-diaminopyrimidin-2-yl)thio]acetic acid
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6-Hydrazinopyrimidine-2,4(1H,3H)-dione
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4-Aminopyrimidine
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