2-METHOXY-5-NITROBENZALDEHYDE
2-METHOXY-5-NITROBENZALDEHYDE Basic information
- Product Name:
- 2-METHOXY-5-NITROBENZALDEHYDE
- Synonyms:
-
- 2-methoxy-5-nitro-benzaldehyd
- AKOS B028867
- 2-METHOXY-5-NITROBENZALDEHYDE
- Benzaldehyde, 2-methoxy-5-nitro-
- 5-Nitro-o-anisaldehyde
- 5-Nitro-o-anisaldehyde
- 4-(4-morpholinyl)-6-[[4-(phenylmethyl)-1-piperazinyl]methyl]-1,3,5-triazin-2-amine
- CAS:
- 25016-02-8
- MF:
- C8H7NO4
- MW:
- 181.15
- Product Categories:
-
- Aldehydes
- C8
- Carbonyl Compounds
- Mol File:
- 25016-02-8.mol
2-METHOXY-5-NITROBENZALDEHYDE Chemical Properties
- 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
- InChI
- 1S/C8H7NO4/c1-13-8-3-2-7(9(11)12)4-6(8)5-10/h2-5H,1H3
- InChIKey
- YWVSKFXYEWMHEO-UHFFFAOYSA-N
- SMILES
- COc1ccc(cc1C=O)[N+]([O-])=O
- CAS DataBase Reference
- 25016-02-8
- EPA Substance Registry System
- Benzaldehyde, 2-methoxy-5-nitro- (25016-02-8)
MSDS
- Language:English Provider:SigmaAldrich
2-METHOXY-5-NITROBENZALDEHYDE Usage And Synthesis
Synthesis
97-51-8
74-88-4
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
2-METHOXY-5-NITROBENZALDEHYDE Preparation Products And Raw materials
Raw materials
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