Other grades of this product :
| Inabenfide Basic information |
| Product Name: | Inabenfide | | Synonyms: | SERITARD;4’-chloro-2’-(alpha-hydroxybenzyl)isonicotinanilide;cgr-811;n-(4-chloro-2-(hydroxyphenylmethyl)phenyl)-4-pyridinecarboxamid;n-(4-chloro-2-(hydroxyphenylmethyl)phenyl)-4-pyridinecarboxamide;INABENFIDE;4′-Chloro-2′-(α-hydroxybenzyl)isonicotinanilide;N-[4-Chloro-2-(hydroxy-phenylmethyl)phenyl]pyridine-4-carboxamide | | CAS: | 82211-24-3 | | MF: | C19H15ClN2O2 | | MW: | 338.79 | | EINECS: | | Product Categories: | pyridine | | Mol File: | 82211-24-3.mol |
| Inabenfide Chemical Properties |
| Melting point | approximate 202℃ (dec.) | | Boiling point | 454.6±45.0 °C(Predicted) | | density | 1.2238 (rough estimate) | | refractive index | 1.5400 (estimate) | | storage temp. | 0-6°C | | pka | 10.77±0.70(Predicted) | | form | neat | | BRN | 7042400 | | CAS DataBase Reference | 82211-24-3(CAS DataBase Reference) |
| WGK Germany | 3 | | HS Code | 29333990 |
| Inabenfide Usage And Synthesis |
| Metabolic pathway | In rats, inabenfide is mainly hydroxylated on the
phenyl ring which is not substituted by a chlorine atom
through epoxidation. Oxidation of the benzyl alcohol
gives benzophenone. The other hydroxylation is the
substitution of the chlorine with hydroxyl of the other phenyl ring possessing a chlorine atom. Also,
hydrolysis of the amide bond resulting in the
corresponding aniline and N-oxidation of the pyridine
nitrogen can be observed. |
| Inabenfide Preparation Products And Raw materials |
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