| Weight | 201.565 g/mol |
|---|---|
| Formula | C7H4ClNO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Nitrophenyl chloroformate (7693-46-1)
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- Re-investigation of the 4-nitrophenyl chloroformate activation of dextran: evidence for the formation of different types of carbonate moieties (Macromolecular Chemistry and Physics, 1985)
- Kinetics of the pH-independent hydrolysis of 4-nitrophenyl chloroformate in aqueous micellar solutions: effects of the charge and structure of the surfactant (Journal of Physical Organic Chemistry, 1999)
- Kinetics of the pHindependent hydrolyses of 4nitrophenyl chloroformate and 4nitrophenyl heptafluorobutyrate in wateracetonitrile mixtures: consequences of solvent composition and ester hydrophobicity (Journal of Physical Organic Chemistry, 2006)
- Activation of poly[N(2hydroxypropyl)methacrylamide] for the binding of bioactive molecules, 1. Activation with 4nitrophenyl chloroformate (Macromolecular Chemistry and Physics, 1983)
- 4-Nitrophenyl Chloroformate: AVersatile Coupling Reagent (Synlett, 2009)
- 9-Fluorenylmethyl chloroformate (Fmoc-Cl) as a useful reagent for the synthesis of pentafluorophenyl, 2,4,5-trichlorophenyl, pentachlorophenyl, p-nitrophenyl, o-nitrophenyl and succinimidyl esters of N -urethane protected amino acids (Letters in Peptide Science, 2003)
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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(=CC=C1[N+](=O)[O-])OC(=O)Cl
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InChIKeyNXLNNXIXOYSCMB-UHFFFAOYSA-N
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