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| | 2-Chloro-3-nitrobenzoic acid Basic information |
| | 2-Chloro-3-nitrobenzoic acid Chemical Properties |
| Melting point | 183-187 °C (lit.) | | Boiling point | 359.9±27.0 °C(Predicted) | | density | 1.6620 | | refractive index | 1.6000 (estimate) | | storage temp. | Sealed in dry,Room Temperature | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Powder | | pka | pK1: 2.02 (25°C) | | color | White to cream-yellow with a green cast | | BRN | 645427 | | InChI | InChI=1S/C7H4ClNO4/c8-6-4(7(10)11)2-1-3-5(6)9(12)13/h1-3H,(H,10,11) | | InChIKey | JRQDVRIQJJPHEQ-UHFFFAOYSA-N | | SMILES | C(O)(=O)C1=CC=CC([N+]([O-])=O)=C1Cl | | CAS DataBase Reference | 3970-35-2(CAS DataBase Reference) |
| | 2-Chloro-3-nitrobenzoic acid Usage And Synthesis |
| Chemical Properties | White to light yellow crystal powder | | Uses | 2-Chloro-3-nitrobenzoic acid is used in a microwave-promoted Ulmann condensation with 2-aminopyridines. | | Uses | 2-Chloro-3-nitrobenzoic acid was used as reagent during the synthesis of new biprivileged molecular scaffolds of tetracyclic indolo-benzodiazepines and indolo-quinoxalines. It was used in a microwave-promoted Ulmann condensation with 2-aminopyridines. | | General Description | 2-Chloro-3-nitrobenzoic acid undergoes condensation with aminoquinolines to yield phenylquinolylamines. |
| | 2-Chloro-3-nitrobenzoic acid Preparation Products And Raw materials |
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