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2-METHOXY-5-NITROBENZALDEHYDE

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Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: CAS:25016-02-8
Purity:0.99 Package:1kg
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Products Intro: Product Name:2-Methoxy-5-nitrobenzaldehyde
CAS:25016-02-8
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CAS:25016-02-8
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CAS:25016-02-8
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Products Intro: Product Name:2-Methoxy-5-nitrobenzaldehyde
CAS:25016-02-8
Purity:98% Package:1g,5g,10g

2-METHOXY-5-NITROBENZALDEHYDE manufacturers

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
EINECS:
Product Categories:Aldehydes;C8;Carbonyl Compounds
Mol File:25016-02-8.mol
2-METHOXY-5-NITROBENZALDEHYDE Structure
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
InChI1S/C8H7NO4/c1-13-8-3-2-7(9(11)12)4-6(8)5-10/h2-5H,1H3
InChIKeyYWVSKFXYEWMHEO-UHFFFAOYSA-N
SMILESCOc1ccc(cc1C=O)[N+]([O-])=O
CAS DataBase Reference25016-02-8
EPA Substance Registry SystemBenzaldehyde, 2-methoxy-5-nitro- (25016-02-8)
Safety Information
WGK Germany 3
TSCA TSCA listed
HS Code 2913000090
Storage Class13 - Non Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
2-METHOXY-5-NITROBENZALDEHYDE Usage And Synthesis
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
2-METHOXY-5-NITROBENZALDEHYDE Preparation Products And Raw materials
Raw materialsMethanol-->Diethyl ether-->Iodomethane-->Silver oxide-->5-Nitrosalicylaldehyde-->2-methoxy-5-nitrobenzonitrile-->Sodium hydride-->N,N-Dimethylformamide
Tag:2-METHOXY-5-NITROBENZALDEHYDE(25016-02-8) Related Product Information
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