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3-METHOXY-4-NITROBENZALDEHYDE

Product Name
3-METHOXY-4-NITROBENZALDEHYDE
CAS No.
80410-57-7
Chemical Name
3-METHOXY-4-NITROBENZALDEHYDE
Synonyms
3-METHOXY-4-NITROBENZALDEHYDE;Benzaldehyde, 3-Methoxy-4-nitro-;3-Methoxy-4-nitrobenzaldehyde 97%
CBNumber
CB7829893
Molecular Formula
C8H7NO4
Formula Weight
181.15
MOL File
80410-57-7.mol
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3-METHOXY-4-NITROBENZALDEHYDE Property

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
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Safety

HS Code 
2912290090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
M266588
Product name
3-methoxy-4-nitrobenzaldehyde
Packaging
50mg
Price
$65
Updated
2021/12/16
Apolloscientific
Product number
OR400210
Product name
3-Methoxy-4-nitrobenzaldehyde
Purity
97%
Packaging
1g
Price
$127
Updated
2021/12/16
SynQuest Laboratories
Product number
4654-1-4M
Product name
3-Methoxy-4-nitrobenzaldehyde
Purity
97%
Packaging
1g
Price
$140
Updated
2021/12/16
Apolloscientific
Product number
OR400210
Product name
3-Methoxy-4-nitrobenzaldehyde
Purity
97%
Packaging
5g
Price
$414
Updated
2021/12/16
SynQuest Laboratories
Product number
4654-1-4M
Product name
3-Methoxy-4-nitrobenzaldehyde
Purity
97%
Packaging
5G
Price
$456
Updated
2021/12/16
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3-METHOXY-4-NITROBENZALDEHYDE Chemical Properties,Usage,Production

Synthesis

704-13-2

74-88-4

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

3-METHOXY-4-NITROBENZALDEHYDE Preparation Products And Raw materials

Raw materials

Preparation Products

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3-METHOXY-4-NITROBENZALDEHYDE Suppliers

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