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| | 2-Amino-3,5-dibromobenzaldehyde Basic information |
| Product Name: | 2-Amino-3,5-dibromobenzaldehyde | | Synonyms: | 3,5-DIBROMOANTHRANILALDEHYDE;3,5-DIBROMANTHRANILALDEHYD;3,5-Dibromo-2-aminobenzaldehyde;2-AMINO-3,5-DIBROMOBENZALDEHYDE 98+%;2-Amino-3,5-Bromo Benzaldehyde;2-AMINO-3,5-DIBROMOBENZALDEHYDE=3,5-DIBROMOANTHRANILALDEHYDE;Benzaldehyde, 2-amino-3,5-dibromo-;2-Amino-3,5-dibromobenzaldehyde,97% | | CAS: | 50910-55-9 | | MF: | C7H5Br2NO | | MW: | 278.93 | | EINECS: | 256-841-0 | | Product Categories: | Aromatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Benzaldehyde;(intermediate of ambroxol hcl);Ambroxol;Aldehydes;C7;Carbonyl Compounds;Aromatic Aldehydes & Derivatives (substituted) | | Mol File: | 50910-55-9.mol |  |
| | 2-Amino-3,5-dibromobenzaldehyde Chemical Properties |
| Melting point | 130-135 °C (lit.) | | Boiling point | 319.9±42.0 °C(Predicted) | | density | 2.0123 (rough estimate) | | refractive index | 1.6400 (estimate) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Solid | | pka | -2.29±0.10(Predicted) | | color | Yellow | | Sensitive | Air Sensitive | | InChIKey | RCPAZWISSAVDEA-UHFFFAOYSA-N | | CAS DataBase Reference | 50910-55-9(CAS DataBase Reference) |
| | 2-Amino-3,5-dibromobenzaldehyde Usage And Synthesis |
| Chemical Properties | Yellow crystalline powder | | Uses | 2-Amino-3,5-dibromobenzaldehyde may be employed in the preparation of tetradentate Schiff base ligands, via condensation with aliphatic diamines. These ligands forms nickel (II) and oxovanadium(IV) complexes. | | Uses | 2-Amino-3,5-dibromobenzaldehyde is a reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites.
| | General Description | 2-Amino-3,5-dibromobenzaldehyde has been identified as one of the oxidation product of bromhexine by controlled potential electrolysis followed by HPLC-UV and GC-MS. It participates in the Friedl?nder condensation of C-β?glycosylic ketones to form 2-substituted quinoline derivatives. |
| | 2-Amino-3,5-dibromobenzaldehyde Preparation Products And Raw materials |
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