Basic information Safety Supplier Related

3-BROMO-5-NITROBENZALDEHYDE

Basic information Safety Supplier Related

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
More
Less

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
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38-43
Safety Statements 
26-36/37
WGK Germany 
3
HS Code 
2913000090
More
Less

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

3-BROMO-5-NITROBENZALDEHYDESupplier

Shanghai Boyle Chemical Co., Ltd.
Tel
Email
sales@boylechem.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Email
isenchem@163.com