| Identification | Back Directory | [Name]
3-BROMO-4-CHLORO-BENZALDEHYDE | [CAS]
86265-88-5 | [Synonyms]
3-BROMO-4-CHLORO-BENZALDEHYDE
Benzaldehyde, 3-bromo-4-chloro- | [Molecular Formula]
C7H4BrClO | [MDL Number]
MFCD08059100 | [MOL File]
86265-88-5.mol | [Molecular Weight]
219.46 |
| Chemical Properties | Back Directory | [Melting point ]
70℃ | [Boiling point ]
277.8±20.0℃ (760 Torr) | [density ]
1.698±0.06 g/cm3 (20 ºC 760 Torr) | [Fp ]
121.8±21.8℃ | [storage temp. ]
Inert atmosphere,2-8°C | [form ]
solid | [color ]
White | [InChI]
InChI=1S/C7H4BrClO/c8-6-3-5(4-10)1-2-7(6)9/h1-4H | [InChIKey]
AKDABJGHOOCVKX-UHFFFAOYSA-N | [SMILES]
C(=O)C1=CC=C(Cl)C(Br)=C1 |
| Hazard Information | Back Directory | [Uses]
3-BROMO-4-CHLORO-BENZALDEHYDE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process. | [Synthesis]
The product from above (3.4 g, 22 mmol) in concentrated 48% aqueous HBr (20 mL) at 0 ??C was treated with a 0 ??C solution of NaNO2 (1.5 g, 22 mmol) in water (30 mL). The reaction mixture was stirred for 30 min and then transferred cold to a stirred solution of CuBr (4.44 g, 31 mmol) in 48% aqueous HBr (20 mL) at 23 ??C (significant frothing!). Water (40 mL) was added, the solution was heated at 60 ??C for 45 min, cooled, diluted with EtOAc (200 mL) and water (50 mL), and the layers were separated. The aqueous layer was extracted with EtOAc (2x, 50 mL). The organic layers were combined, washed with 1 M HCl (2x, 100 mL) and brine (50 mL), dried (Na2SO4), filtered, and concentrated to provide 3-bromo-4-chlorobenzaldehyde as a pale yellow powder (3.9 g, 82%). 3-Bromo-4-chlorobenzaldehyde, yield 3.9 g, 82% | [References]
[1] Patent: US2003/83357, 2003, A1
[2] Patent: US6515003, 2003, B1
[3] Patent: US2006/154915, 2006, A1. Location in patent: Page/Page column 29
[4] Patent: WO2003/99776, 2003, A1. Location in patent: Page 63 |
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J & K SCIENTIFIC LTD.
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Energy Chemical
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Jia Xing Isenchem Co.,Ltd
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