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| | 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE Basic information |
| Product Name: | 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE | | Synonyms: | 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE;4-Bromo-3-(trifluoromethyl)benzaldehyde 99%;2-Bromo-5-formylbenzotrifluoride;3-(Trifluoromethyl)-4-bromobenzaldehyde;Benzaldehyde, 4-broMo-3-(trifluoroMethyl)-;2-Bromo-5-formylbenzotrifluoride, 4-Bromo-alpha,alpha,alpha-trifluoro-m-tolualdehyde;4-dibromo-3-(trifluoromethyl)benzaldehyde;4-bromo-3-(trifloromethyl)benzaldehyde | | CAS: | 34328-47-7 | | MF: | C8H4BrF3O | | MW: | 253.02 | | EINECS: | | | Product Categories: | | | Mol File: | 34328-47-7.mol |  |
| | 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE Chemical Properties |
| Melting point | 51-54℃ | | Boiling point | 237℃ | | density | 1.677 | | Fp | 97 | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | crystalline powder | | color | Pale lemon |
| | 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE Usage And Synthesis |
| Synthesis | Example 12 Preparation of 4-bromo-3-(trifluoromethyl)benzaldehyde (C70): to a solution of (4-bromo-3-(trifluoromethyl)phenyl)methanol (C72) (12.0 g, 47.1 mmol) in dichloromethane (100 mL) was added manganese dioxide (25.6 g, 294 mmol). The reaction mixture was stirred at room temperature for 12 hours before being filtered through a Celite pad to remove solid impurities. The filtrate was concentrated under reduced pressure to afford 3-trifluoromethyl-4-bromobenzaldehyde as a light yellow solid (10.0 g, 82% yield). The product was characterized by the following data: 1H NMR (300 MHz, CDCl3) δ10.05 (s, 1H), 8.19 (s, 1H), 7.94-7.88 (m, 2H); IR (thin film) 1704, 1123 cm-1; EIMS m/z 219 ([M]+). | | References | [1] Patent: US2018/279612, 2018, A1. Location in patent: Paragraph 0382-0383 |
| | 4-BROMO-3-TRIFLUOROMETHYL-BENZALDEHYDE Preparation Products And Raw materials |
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