| Weight | 108.104 g/mol |
|---|---|
| Formula | C4H4N4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
16617-46-2 (16617-46-2)
5-amino-4-cyanopyrazole
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- Synthesis of N-aryl-5-amino-4-cyanopyrazole derivatives as potent xanthine oxidase inhibitors. (European Journal of Medicinal Chemistry, 2008)
- A simplified green chemistry approaches to synthesis of 2-substituted 1,2,3-triazoles and 4-amino-5-cyanopyrazole derivatives conventional heating versus microwave and ultrasound as ecofriendly energy sources. (Ultrasonics Sonochemistry, 2009)
- Nitropyrazoles: 5. Synthesis of substituted 3-nitropyrazoles from 3-amino-4-cyanopyrazole (Russian Chemical Bulletin, 1993)
- Discovery of novel non-carboxylic acid 5-amino-4-cyanopyrazole derivatives as potent and highly selective LPA1R antagonists (Bioorganic & Medicinal Chemistry Letters, 2014)
- Synthesis and crystal structure of 1-(1,3-dimethyl-5-chloropyrazol-4-carbonyl-3-(2-chlorophenyl)-5-amino-4-cyanopyrazole (Journal of Chemical Crystallography, 2000)
- Synthesis and Crystal Structure of 1-(2,6-Dichloro-4-nitrophenyl)-5-amino-4-cyanopyrazole (Chinese Journal of Structural Chemistry, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-amino-4-cyanopyrazole
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SMILESC1=NNC(=C1C#N)N
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InChIKeyFFNKBQRKZRMYCL-UHFFFAOYSA-N
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