ChemicalBook--->CAS DataBase List--->25016-02-8

25016-02-8

25016-02-8 Structure

25016-02-8 Structure
IdentificationBack Directory
[Name]

2-METHOXY-5-NITROBENZALDEHYDE
[CAS]

25016-02-8
[Synonyms]

AKOS B028867
5-Nitro-o-anisaldehyde
5-Nitro-o-anisaldehyde
2-METHOXY-5-NITROBENZALDEHYDE
2-methoxy-5-nitro-benzaldehyd
Benzaldehyde, 2-methoxy-5-nitro-
4-(4-morpholinyl)-6-[[4-(phenylmethyl)-1-piperazinyl]methyl]-1,3,5-triazin-2-amine
[Molecular Formula]

C8H7NO4
[MDL Number]

MFCD02093683
[MOL File]

25016-02-8.mol
[Molecular Weight]

181.15
Chemical PropertiesBack Directory
[Melting point ]

89-92 °C(lit.)
[Boiling point ]

336.7±27.0 °C(Predicted)
[density ]

1.322±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

very soluble in Dimethylformamide
[form ]

powder to crystal
[color ]

White to Light yellow to Light orange
[CAS DataBase Reference]

25016-02-8
[EPA Substance Registry System]

Benzaldehyde, 2-methoxy-5-nitro- (25016-02-8)
Safety DataBack Directory
[WGK Germany ]

3
[TSCA ]

TSCA listed
[HS Code ]

2913000090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Diethyl ether-->Iodomethane-->Silver oxide-->5-Nitrosalicylaldehyde-->2-methoxy-5-nitrobenzonitrile-->Sodium hydride-->N,N-Dimethylformamide
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXY-5-NITROBENZALDEHYDE(25016-02-8)1HNMR
2-METHOXY-5-NITROBENZALDEHYDE(25016-02-8)IR
Hazard InformationBack Directory
[Synthesis]

5-Nitrosalicylaldehyde

97-51-8

Iodomethane

74-88-4

2-METHOXY-5-NITROBENZALDEHYDE

25016-02-8

General procedure for the synthesis of 2-methoxy-5-nitrobenzaldehyde from 5-nitrosalicylaldehyde and iodomethane: Sodium hydride (NaH, 246 mg) and iodomethane (2.56 g) were added to a solution of 5-nitrosalicylaldehyde (1.00 g, 6.0 mmol) in N,N-dimethylformamide (DMF, 20 ml). The reaction mixture was stirred at 0°C for 8.5 hours. After completion of the reaction, the reaction mixture was extracted with ether and the organic phase was washed sequentially with aqueous sodium bicarbonate, saturated brine and 5% hydrochloric acid/saturated brine. The organic phase was dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give 2-methoxy-5-nitrobenzaldehyde (0.95 g, 87.8% yield) as yellow needle-like crystals. The product was characterized by 1H NMR (CDCl3): δ 10.45 (s, 1H), 8.70 (d, J = 2.9Hz, 1H), 8.45 (dd, J = 8.8, 2.9Hz, 1H), 7.14 (d, J = 8.8Hz, 1H), 4.08 (s, 3H).

[References]

[1] Angewandte Chemie - International Edition, 2011, vol. 50, # 15, p. 3435 - 3438
[2] Patent: US2013/261295, 2013, A1. Location in patent: Paragraph 0166; 0167
[3] Journal of the American Chemical Society, 2017, vol. 139, # 19, p. 6654 - 6662
[4] Patent: US5837711, 1998, A
[5] Journal of the Chemical Society, 1951, p. 2462,2466
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