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79025-28-8

79025-28-8 Structure

79025-28-8 Structure
IdentificationBack Directory
[Name]

3,4-diMethoxy-2-nitrobenzoic acid
[CAS]

79025-28-8
[Synonyms]

2-Nitroveratric acid
3,4-diMethoxy-2-nitrobenzoic acid
Benzoic acid, 3,4-diMethoxy-2-nitro-
[Molecular Formula]

C9H9NO6
[MDL Number]

MFCD00074884
[MOL File]

79025-28-8.mol
[Molecular Weight]

227.17
Chemical PropertiesBack Directory
[Melting point ]

200-202℃
[Boiling point ]

399.5±42.0 °C(Predicted)
[density ]

1.403
[storage temp. ]

2-8°C
[pka]

2.34±0.25(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

3,4-diMethoxy-2-nitrobenzoic acid(79025-28-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzaldehyde, 3,4-diMethoxy-2-nitro-

55149-84-3

3,4-diMethoxy-2-nitrobenzoic acid

79025-28-8

Example 76: In the preparation of 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid {1-[2-(7,8-dimethoxyquinoxalin-2-ylthioalkyl)ethyl]piperidin-4-yl}amide, 3,4-dimethoxy-2-nitrobenzoic acid was synthesized as follows: to a stirred 3,4-dimethoxy-2-nitrobenzaldehyde at room temperature (0.4 g, 1.9 mmol, 1.0 eq.) of acetic acid (10 mL) solution was added potassium permanganate (0.6 g, 3.8 mmol, 2.0 eq.). The reaction mixture was stirred overnight at room temperature before being quenched with saturated aqueous sodium sulfite solution and extracted with ethyl acetate (3 x 20 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated to give 3,4-dimethoxy-2-nitrobenzoic acid (0.35 g, 81% yield) as a white solid. The product was characterized by 1H-NMR (400 MHz, acetone-d6) and mass spectrometry (-ESI): 1H-NMR δ 7.86 (d, J=8.8 Hz, 1H), 7.34 (d, J=8.8 Hz, 1H), 4.06 (s, 3H), 3.89 (s, 3H); MS m/z: 226.1 [M-H]-.

[References]

[1] Journal of Chemical Research, Miniprint, 1990, # 12, p. 2831 - 2867
[2] Patent: WO2010/84152, 2010, A1. Location in patent: Page/Page column 120-121
[3] MedChemComm, 2014, vol. 5, # 9, p. 1290 - 1296
[4] Chemische Berichte, 1910, vol. 43, p. 2140
[5] Journal of the Chemical Society, 1954, p. 2246,2255
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