ChemicalBook--->CAS DataBase List--->15969-08-1

15969-08-1

15969-08-1 Structure

15969-08-1 Structure
IdentificationBack Directory
[Name]

2-METHOXY-6-NITROPHENOL
[CAS]

15969-08-1
[Synonyms]

2-METHOXY-6-NITROPHENOL
6-methoxy-2-nitrophenol
Phenol, 2-methoxy-6-nitro-
[Molecular Formula]

C7H7NO4
[MDL Number]

MFCD08693430
[MOL File]

15969-08-1.mol
[Molecular Weight]

169.13
Chemical PropertiesBack Directory
[Melting point ]

62 °C (sublm)
[Boiling point ]

260.3±20.0 °C(Predicted)
[density ]

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

Inert atmosphere,Room Temperature
[pka]

7.09±0.24(Predicted)
[Appearance]

Yellow to orange Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2906290090
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXY-6-NITROPHENOL(15969-08-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Guaiacol

90-05-1

2-methoxy-3-nitrophenol

20734-71-8

2-METHOXY-6-NITROPHENOL

15969-08-1

General procedure for the synthesis of 2-methoxy-3-nitrophenol and 6-methoxy-2-nitrophenol from guaiacol: Fuming HNO3 (0.34 mL, 0.008 mmol) was slowly added dropwise to a solution of 2-methoxyphenol (0.886 mL, 0.008 mmol) dissolved in anhydrous dichloromethane (10 mL) at -20 °C. The reaction mixture was stirred continuously for 2 hours at room temperature. Subsequently, the reaction mixture was concentrated under reduced pressure to remove the solvent. Separation by column chromatography (eluent ratio 10-30% ethyl acetate/hexane) afforded the target products 2-methoxy-3-nitrophenol (400 mg, 29% yield) and 6-methoxy-2-nitrophenol (400 mg, 29% yield).

[References]

[1] Patent: US2007/93477, 2007, A1. Location in patent: Page/Page column 27
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