| Weight | 124.099 g/mol |
|---|---|
| Formula | C5H4N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Pyrimidine-5-carboxylic acid (4595-61-3)
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- Synthesis of 7-Substituted 5-Oxo-5H-thiazolo[3,2-a]pyrimidine-6-carboxylic Acids, 2-Substituted 4-Oxo-4H-pyrido [1,2-a]pyrimidine-3-carboxylic Acids, and 2,6-Disubstituted 4-Quinolones from Meldrum's Acid (Synthesis, 1989)
- Solventfree synthesis of 5methyl7aryl4,7dihydrotetrazolo[1,5a]pyrimidine6carboxylic esters catalyzed by sulfamic acid (Journal of Heterocyclic Chemistry, 2008)
- Analogs of tetrahydrofolic acid. XXVI. synthesis of some 5-aryl and 5-aralkyl pyrimidine-6-carboxylic acids and their effect on dihydrofolic reductase and thymidylate synthetase (Journal of Heterocyclic Chemistry, 1965)
- Triorganotin(IV) derivatives of 7-amino-2-(methylthio)[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylic acid. Synthesis, spectroscopic characterization, in vitro antimicrobial activity and X-ray crystallography (Journal of Organometallic Chemistry, 2010)
- Certain 2-substituted-5,8-dihydro-5-oxopyrido{8 2,3-d{9 pyrimidine-6-carboxylic acid derivatives (1970)
- Fluorinated 1,2,4-Triazolo[1,5-a]pyrimidine-6-carboxylic Acid Derivatives as Antimycobacterial Agents (Archiv Der Pharmazie, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C=NC=N1)C(=O)O
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InChIKeyIIVUJUOJERNGQX-UHFFFAOYSA-N
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Pyrimidine-5-carboxylic acid
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