| Weight | 246.562 g/mol |
|---|---|
| Formula | C7H3ClN2O6 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
4-CHLORO-3,5-DINITROBENZOIC ACID (118-97-8)
4-chloro-3,5-dinitrobenzoate
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- Definition of cytochrome c binding domains by chemical modification. I. Reaction with 4-chloro-3,5-dinitrobenzoate and chromatographic separation of singly substituted derivatives. (Journal of Biological Chemistry, 1978)
- The spectroscopic (FT-Raman, FT-IR, UV and NMR), molecular electrostatic potential, polarizability and hyperpolarizability, NBO and HOMOLUMO analysis of monomeric and dimeric structures of 4-chloro-3,5-dinitrobenzoic acid (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- Hydroxyl radical initiated photodegradation of 4-chloro-3,5-dinitrobenzoic acid in aqueous solution (Journal of Photochemistry and Photobiology A-chemistry, 2000)
- Chemical modification of spinach plastocyanin using 4-chloro-3,5-dinitrobenzoic acid: characterization of four singly-modified forms. (Biochimica et Biophysica Acta, 1990)
- Preparation of a new chiral stationary phase for HPLC based on the (R)- 1-phenyl-2-(4-methylphenyl)ethylamine amide derivative of (S)-valine and 2-chloro-3,5-dinitrobenzoic acid: enantioseparation of amino acid derivatives and pyrethroid insecticides. (Journal of Separation Science, 2007)
- Enantiomer Separation and Molecular Recognition with New Chiral Stationary Phases on 4Chloro3,5dinitrobenzoic Acid Amides of ,Aminoalcohols and Arylethylamines (Journal of Liquid Chromatography & Related Technologies, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-chloro-3,5-dinitrobenzoate
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SMILESC1=C(C=C(C(=C1[N+](=O)[O-])Cl)[N+](=O)[O-])C(=O)O
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InChIKeyPCTFIHOVQYYAMH-UHFFFAOYSA-N
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