3-METHOXY-4-NITROBENZALDEHYDE

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Products Intro: Product Name:3-Methoxy-4-nitrobenzaldehyde
CAS:80410-57-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-22237
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Products Intro: Product Name:3-METHOXY-4-NITROBENZALDEHYDE
CAS:80410-57-7
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CAS:80410-57-7
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Products Intro: Product Name:3-Methoxy-4-nitrobenzaldehyde
CAS:80410-57-7
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Products Intro: Product Name:3-methoxy-4-nitrobenzaldehyde
CAS:80410-57-7
Purity:0.98 Package:100KG;25KG;10KG;1KG
3-METHOXY-4-NITROBENZALDEHYDE Basic information
Product Name:3-METHOXY-4-NITROBENZALDEHYDE
Synonyms:3-METHOXY-4-NITROBENZALDEHYDE;Benzaldehyde, 3-Methoxy-4-nitro-;3-Methoxy-4-nitrobenzaldehyde 97%
CAS:80410-57-7
MF:C8H7NO4
MW:181.15
EINECS:
Product Categories:
Mol File:80410-57-7.mol
3-METHOXY-4-NITROBENZALDEHYDE Structure
3-METHOXY-4-NITROBENZALDEHYDE Chemical Properties
Melting point 104 °C
Boiling point 354.7±27.0 °C(Predicted)
density 1.322±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form crystalline powder
color Cream/gold/faint tan
Safety Information
HS Code 2912290090
MSDS Information
3-METHOXY-4-NITROBENZALDEHYDE Usage And Synthesis
Synthesis
3-Hydroxy-4-nitrobenzaldehyde

704-13-2

Iodomethane

74-88-4

3-METHOXY-4-NITROBENZALDEHYDE

80410-57-7

(1) Synthesis of 3-methoxy-4-nitrobenzaldehyde: 3-hydroxy-4-nitrobenzaldehyde (500 mg, 2.99 mmol) and potassium carbonate (0.42 g, 3.0 mmol) were dissolved in 6.0 mL of N,N-dimethylformamide. Iodomethane (0.38 mL, 6.0 mmol) was slowly added to the reaction system at room temperature, followed by continuous stirring at the same temperature for 5 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate and water and separated. The organic layer was washed twice with saturated brine and subsequently dried with anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate = 4/1 to 1/1) to afford the target compound, 3-methoxy-4-nitrobenzaldehyde, as a light yellow powder (518 mg, 96% yield).

References[1] ACS Medicinal Chemistry Letters, 2017, vol. 8, # 10, p. 1002 - 1006
[2] Patent: WO2016/124747, 2016, A1. Location in patent: Page/Page column 62; 63
[3] Patent: US2018/202388, 2018, A1
[4] Patent: EP2123637, 2009, A1. Location in patent: Page/Page column 19
[5] Organic and Biomolecular Chemistry, 2014, vol. 12, # 30, p. 5629 - 5633
Tag:3-METHOXY-4-NITROBENZALDEHYDE(80410-57-7) Related Product Information
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