| Weight | 227.219 g/mol |
|---|---|
| Formula | C13H9NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
4-Nitrobenzophenone (1144-74-7)
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- Active esters of polymer-bound 4-hydroxy-3-nitrobenzophenone as useful acylating reagents. Application to peptide synthesis (Journal of Organic Chemistry, 1984)
- Spectral and electrochemical studies of ruthenium(II) complexes with N4-methyl-4-nitrobenzaldehyde and N4-methyl-4-nitrobenzophenone thiosemicarbazone : Potential anti-trypanosomal agents (Polyhedron, 2008)
- A NEW AND CONVENIENT SYNTHESIS OF 4-AMINO-3-NITROBENZOPHENONE AND 2-AMINO-5-NITROBENZOPHENONE AND THEIR N-ALKYL DERIVATIVES (Organic Preparations and Procedures International, 1987)
- Manganese(II) complexes with N4-methyl-4-nitrobenzaldehyde, N4-methyl-4-nitroacetofenone, and N4-methyl-4-nitrobenzophenone thiosemicarbazone: Investigation of in vitro activity against Trypanosoma cruzi (Polyhedron, 2010)
- Experimental study on the thermochemistry of 3-nitrobenzophenone, 4-nitrobenzophenone and 3,3-dinitrobenzophenone (The Journal of Chemical Thermodynamics, 2011)
- Reduction mechanism of 4-nitrobenzophenone in tetrahydrofuran. Influence of added proton donors (Canadian Journal of Chemistry, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)[N+](=O)[O-]
-
InChIKeyZYMCBJWUWHHVRX-UHFFFAOYSA-N
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