| Weight | 141.082 g/mol |
|---|---|
| Formula | C5H3NO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
5-Nitrofurfural (698-63-5)
5-nitro-2-furaldehyde · 5-nitrofuraldehyde
Score:
#4109 in Biology
,
#5175 in Chemistry
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- Synthesis and antitrypanosomal evaluation of E-isomers of 5-nitro-2-furaldehyde and 5-nitrothiophene-2-carboxaldehyde semicarbazone derivatives. Structure-activity relationships. (European Journal of Medicinal Chemistry, 2000)
- Synthesis and anti-trypanosomal activity of novel 5-nitro-2-furaldehyde and 5-nitrothiophene-2-carboxaldehyde semicarbazone derivatives (Farmaco, 1998)
- An efficient microwave-assisted method to obtain 5-nitrofurfural without solvents on mineral solid supports (Tetrahedron Letters, 1995)
- THE CHEMOTHERAPEUTIC PROPERTIES OF 5-NITRO-2-FURALDEHYDE SEMICARBAZONE (FURACIN) (Journal of Pharmacology and Experimental Therapeutics, 1946)
- Transplantable Rat Mammary Tumors Induced by 5-Nitro-2-furaldehyde Semicarbazone and by Formic Acid 2-[4-(5-Nitro-2-furyl)-2-thiazolyl]hydrazide (Cancer Research, 1970)
- Antibacterial nitrofuran derivatives. 2. 5-Nitro-2-furaldehyde aminoacethydrazones (Journal of Medicinal Chemistry, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-nitro-2-furaldehyde
- 5-nitrofuraldehyde
-
SMILESC1=C(OC(=C1)[N+](=O)[O-])C=O
-
InChIKeySXINBFXPADXIEY-UHFFFAOYSA-N
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Similar Compounds
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5-Nitrofurfural
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