3-BROMO-5-NITROBENZALDEHYDE
3-BROMO-5-NITROBENZALDEHYDE Basic information
- Product Name:
- 3-BROMO-5-NITROBENZALDEHYDE
- Synonyms:
-
- 3-BROMO-5-NITROBENZALDEHYDE
- 3-Bromo-5-nitrobenzaldehyde 95%
- 3-Fluoro-5-nitrobenzaldehyde
- Benzaldehyde,3-bromo-5-nitro-
- 3-BroMo-5-nitrobenzaldehyde, 97+%
- 3-Bromo-5-formylnitrobenzene
- 3-Nitro-5-bromo-benzaldehyde
- CAS:
- 355134-13-3
- MF:
- C7H4BrNO3
- MW:
- 230.02
- Product Categories:
-
- Nitro CompoundsChemical Synthesis
- Aldehydes
- C7Organic Building Blocks
- Carbonyl Compounds
- New Products for Chemical Synthesis
- Nitrogen Compounds
- Organic Building Blocks
- Mol File:
- 355134-13-3.mol
3-BROMO-5-NITROBENZALDEHYDE Chemical Properties
- Melting point:
- 101-106 °C
- Boiling point:
- 306.9±27.0 °C(Predicted)
- Density
- 1.781
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- soluble in Methanol
- form
- Powder
- color
- Pale brown
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38-43
- Safety Statements
- 26-36/37
- WGK Germany
- 3
- HS Code
- 2913000090
3-BROMO-5-NITROBENZALDEHYDE Usage And Synthesis
Uses
3-Fluoro-5-nitrobenzaldehyde is used as a reactant in the design and synthesis of selective activators of cardiac myosin.
Synthesis Reference(s)
The Journal of Organic Chemistry, 72, p. 5867, 2007 DOI: 10.1021/jo070477u
Synthesis
99-61-6
355134-13-3
General procedure for the synthesis of 3-bromo-5-nitrobenzaldehyde from m-nitrobenzaldehyde: 3-nitrobenzaldehyde (1.0 g, 6.6 mmol) was dissolved in concentrated sulfuric acid (4.0 mL) at room temperature, followed by batchwise addition of N-bromosuccinimide (1.4 g, 7.9 mmol). The reaction mixture was heated to 65 °C and maintained at this temperature for 1 hour. After completion of the reaction, it was cooled to room temperature and the reaction solution was slowly poured into ice water, the solid was precipitated and collected by filtration. The crude product was dried with anhydrous sodium sulfate and purified by recrystallization through a solvent mixture of ethyl acetate/petroleum ether (1:10, v/v) to finally obtain 3-bromo-5-nitrobenzaldehyde (1.3 g, 82% yield) as white crystals. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 10.09 (s, 1H), 8.79-8.55 (m, 2H), 8.51 (s, 1H).
References
[1] Journal of Medicinal Chemistry, 2018, vol. 61, # 12, p. 5235 - 5244
[2] Journal of Organic Chemistry, 2007, vol. 72, # 15, p. 5867 - 5869
[3] European Journal of Medicinal Chemistry, 2016, vol. 116, p. 46 - 58
[4] Journal of the American Chemical Society, 2007, vol. 129, # 15, p. 4512 - 4513
[5] Patent: WO2009/153313, 2009, A1. Location in patent: Page/Page column 185
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