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Product Introduction
2-Bromo-N-methylaniline can be synthesized via the reduction of 2-bromoformylanilide.
Application
2-Bromo-N-methylaniline can be used to synthesize benzimidazole derivatives, via one pot N-arylation of amides/cyclic amides in the presence of copper iodide nanoparticles. It can also be used in the synthesis of alkyltelluro-substituted aromatic amines, which can show radical trapping ability.
| CAS | 6832-87-7 |
|---|---|
| Synonymes | A867065 | SY246165 | DS-17555 | 2-Bromo-N-methylaniline | 2-Bromo-N-methylaniline, 95% | AKOS000253684 | DTXSID80318993 | V10176 | 2-bromo-N-methylbenzenamine | SCHEMBL989524 | MFCD06798064 | NSC338420 | NSC-338420 | FT-0696143 | SMVIAQFTVWDWDS-UHFFFAOYSA |
| Spécifications et pureté | ≥96% |
| Conditions de stockage de stockage | Store at 2-8°C |
| Expédié en | Wet ice |
| Product Description | Product Introduction 2-Bromo-N-methylaniline can be synthesized via the reduction of 2-bromoformylanilide. Application 2-Bromo-N-methylaniline can be used to synthesize benzimidazole derivatives, via one pot N-arylation of amides/cyclic amides in the presence of copper iodide nanoparticles. It can also be used in the synthesis of alkyltelluro-substituted aromatic amines, which can show radical trapping ability. |
| Pubchem Sid | 504758502 |
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758502 |
| Numéro CE | 626-537-6 |
| PubChem CID | 334086 |
| Formule moléculaire | C7H8BrN |