ChemicalBook--->CAS DataBase List--->15174-02-4

15174-02-4

15174-02-4 Structure

15174-02-4 Structure
IdentificationBack Directory
[Name]

4-HYDROXY-2-NITRO-ANISOLE
[CAS]

15174-02-4
[Synonyms]

4-METHOXY-3-NITRO-PHENOL
Phenol,4-Methoxy-3-nitro-
4-HYDROXY-2-NITRO-ANISOLE
4-Methoxy-3-nitrophenol@100 μg/mL in Methanol
4-HYDROXY-2-NITRO-ANISOLE ISO 9001:2015 REACH
4-METHOXY-3-NITRO-PHENOL (4-HYDROXY-2-NITRO-ANISOLE)
[Molecular Formula]

C7H7NO4
[MDL Number]

MFCD00031284
[MOL File]

15174-02-4.mol
[Molecular Weight]

169.13
Chemical PropertiesBack Directory
[Boiling point ]

340.5±27.0 °C(Predicted)
[density ]

1.367±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly, Heated, Sonicated)
[form ]

Solid
[pka]

8.67±0.10(Predicted)
[color ]

Light Brown to Dark Beige
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2909500090
Spectrum DetailBack Directory
[Spectrum Detail]

4-HYDROXY-2-NITRO-ANISOLE(15174-02-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-methoxy-3-nitrophenylacetate

39653-87-7

4-HYDROXY-2-NITRO-ANISOLE

15174-02-4

4-Methoxy-3-nitrophenyl acetate (1.06 g, 5 mmol) was dissolved in ethanol (20 mL) at 0 °C and 1N aqueous sodium hydroxide solution (5.5 mL) was slowly added. The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the reaction was quenched with acetic acid and subsequently extracted twice with ethyl acetate. The organic layers were combined, washed sequentially with water and saturated saline, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the crude product 4-hydroxy-2-nitroanisole (840 mg, quantitative yield). Thin layer chromatography (TLC) showed an Rf value of 0.59 (ethyl acetate: hexane= 3:7). NMR hydrogen spectrum (400 MHz, CDCl3) data were as follows: δ 3.91 (s, 3H), 6.99 (d, 1H, J = 9.04Hz), 7.17 (dd, 1H, J = 9.04,3.00Hz), 7.38 (d, 1H, J = 3.04Hz).

[References]

[1] Patent: WO2004/80980, 2004, A1. Location in patent: Page 136
[2] Patent: WO2016/91845, 2016, A1. Location in patent: Page/Page column 83
[3] Monatshefte fuer Chemie, 1914, vol. 35, p. 95
[4] Patent: WO2006/44823, 2006, A2. Location in patent: Page/Page column 165
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