| Weight | 212.252 g/mol |
|---|---|
| Formula | C13H12N2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
3,4-Diaminobenzophenone (39070-63-8)
3,4-diamino benzophenone
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- A matrix of 3,4-diaminobenzophenone for the analysis of oligonucleotides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (Nucleic Acids Research, 2006)
- Scaled quantum chemical calculations and FTIR, FT-Raman spectral analysis of 3,4-diamino benzophenone (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2005)
- Structural Characterization and Properties of Organo-soluble Polyimides, Bismaleimide and Polyaspartimides Based on 4,4-Dichloro-3,3-Diamino Benzophenone (High Performance Polymers, 2006)
- Tetradentate Schiff base ligands of 3,4-diaminobenzophenone: Synthesis, characterization and thermodynamics of complex formation with Ni(II), Cu(II) and Zn(II) metal ions (Journal of The Serbian Chemical Society, 2011)
- Fullerene-Modified Polyimide Derived from 3,3',4',-Benzophenonetetracarboxylic Acid and 3,3'-Diaminobenzophenone for Casted Items and Its Use in Tribology (Russian Journal of Applied Chemistry, 2003)
- Synthesis, characterization, EPR, electrochemical, and in situ spectroelectrochemical studies of salen-type oxovanadium(IV) and copper(II) complexes derived from 3,4-diaminobenzophenone (Journal of Coordination Chemistry, 2013)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,4-diamino benzophenone
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SMILESC1=CC=C(C=C1)C(=O)C2=CC(=C(C=C2)N)N
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InChIKeyRXCOGDYOZQGGMK-UHFFFAOYSA-N
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3,4-Diaminobenzophenone
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