| Weight | 180.188 g/mol |
|---|---|
| Formula | C7H4N2O2S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Nitrophenyl isothiocyanate (2131-61-5)
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- Liquid chromatographic enantioseparation of -blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agent (Journal of Chromatography A, 2001)
- High-performance liquid chromatographic separation of unusual amino acid enantiomers derivatized with (1s, 2s)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl-isothiocyanate (Chromatographia, 2000)
- INDIRECT HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC ENANTIOSEPARATION OF RECEMIC AMINO ALCOHOLS WITH 1,3-DIACETOXY-1-(4-NITROPHENYL)-2-PROPYL ISOTHIOCYANATE AS DERIVATIZING AGENT (Journal of Liquid Chromatography & Related Technologies, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1N=C=S)[N+](=O)[O-]
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InChIKeyNXHSSIGRWJENBH-UHFFFAOYSA-N
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