ChemicalBook--->CAS DataBase List--->67853-37-6

67853-37-6

67853-37-6 Structure

67853-37-6 Structure
IdentificationMore
[Name]

2-Bromo-3-nitroanisole
[CAS]

67853-37-6
[Synonyms]

2-BROMO-1-METHOXY-3-NITROBENZENE
2-BROMO-3-NITROANISOLE
TIMTEC-BB SBB008642
2-Bromo-3-nitroanisole 99%
2-Bromo-3-methoxynitrobenzene
[Molecular Formula]

C7H6BrNO3
[MDL Number]

MFCD07779272
[Molecular Weight]

232.03
[MOL File]

67853-37-6.mol
Chemical PropertiesBack Directory
[Boiling point ]

273.3±20.0 °C(Predicted)
[density ]

1.640±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

powder
[color ]

Yellow
[InChI]

InChI=1S/C7H6BrNO3/c1-12-6-4-2-3-5(7(6)8)9(10)11/h2-4H,1H3
[InChIKey]

KCFDURKFXBLIAY-UHFFFAOYSA-N
[SMILES]

C1(OC)=CC=CC([N+]([O-])=O)=C1Br
[CAS DataBase Reference]

67853-37-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P501
[Hazard Codes ]

Xi
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[HS Code ]

2909309090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Bromo-3-nitroanisole(67853-37-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromo-3-nitrophenol

101935-40-4

Iodomethane

74-88-4

2-Bromo-3-nitroanisole

67853-37-6

General procedure for the synthesis of 2-bromo-3-nitroanisole from 2-bromo-3-nitrophenol (3.1 g, 14.2 mmol) and iodomethane (2.6 mL, 42.5 mmol): 2-bromo-3-nitrophenol was dissolved in N,N-dimethylformamide (DMF, 20 mL), to which was added ground cesium carbonate (5.58 g, 17.1 mmol), followed by the addition of iodomethane. The reaction mixture was stirred at room temperature overnight. After completion of the reaction, DMF was removed by rotary evaporator and the residue was dissolved in ether (200 mL) and washed sequentially with water (200 mL) and saturated sodium chloride solution (4 x 100 mL). The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated to give the crude product 2-bromo-3-nitroanisole (94% yield, 3.1 g) as an orange solid. Mass spectrometry (MS) analysis showed m/z 234 ([M+2H]+). High performance liquid chromatography (HPLC, TFA system, 220 nm detection) showed a product purity of 98%.

[References]

[1] Patent: WO2004/103996, 2004, A1. Location in patent: Page 40-41
[2] Patent: WO2006/7700, 2006, A1. Location in patent: Page/Page column 62
[3] Patent: US2006/19905, 2006, A1. Location in patent: Page/Page column 24
[4] Patent: WO2006/85, 2006, A1. Location in patent: Page/Page column 75-76
[5] Patent: WO2007/9227, 2007, A1. Location in patent: Page/Page column 35
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