| Weight | 304.214 g/mol |
|---|---|
| Formula | C13H8N2O7 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Bis(4-nitrophenyl) carbonate (5070-13-3)
bis(4-nitrophenyl)carbonate
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- Kinetic study of the phenolysis of bis(4-nitrophenyl) carbonate, bis(4-nitrophenyl) thionocarbonate, and methyl 4-nitrophenyl thionocarbonate. (Journal of Organic Chemistry, 2001)
- Kinetics and mechanism of the aminolysis of bis(4-nitrophenyl) carbonate and O-(4-nitropheny) S-(4-nitrophenyl) thio and dithiocarbonate (Journal of Physical Organic Chemistry, 2014)
- Atypical deacylation of the acyl enzymes formed in the reaction of .alpha.-chymotrypsin with bis(4-nitrophenyl) carbonate and o-(4-nitrophenylene) carbonate (Journal of the American Chemical Society, 1972)
- HYDROLYSIS OF BIS(4-NITROPHENYL) CARBONATE AND THE GENERAL BASE CATALYZED HYDROLYSIS OF o-(4-NITROPHENYLENE) CARBONATE. (Journal of Organic Chemistry, 1970)
- Electronic and structural effects on the nonlinear optical behavior in conjugated structure bis(4nitrophenyl) carbonate: a vibrational spectroscopic approach (Journal of Raman Spectroscopy, 2011)
- Activation of Supports Containing Hydroxyl Groups Using bis(4-Nitrophenyl) carbonate (Analytical Letters, 1996)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bis(4-nitrophenyl)carbonate
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SMILESC1=CC(=CC=C1[N+](=O)[O-])OC(=O)OC2=CC=C(C=C2)[N+](=O)[O-]
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InChIKeyACBQROXDOHKANW-UHFFFAOYSA-N
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