4-NITROPHENYL-2-METHOXYETHYL ETHER
- Product Name
- 4-NITROPHENYL-2-METHOXYETHYL ETHER
- CAS No.
- 22483-40-5
- Chemical Name
- 4-NITROPHENYL-2-METHOXYETHYL ETHER
- Synonyms
- SKL382;1-(2-Methoxyethoxy);4-NITROPHENYL-2-METHOXYETHYL ETHER;Benzene, 1-(2-methoxyethoxy)-4-nitro-
- CBNumber
- CB1789113
- Molecular Formula
- C9H11NO4
- Formula Weight
- 197.19
- MOL File
- 22483-40-5.mol
4-NITROPHENYL-2-METHOXYETHYL ETHER Property
- Melting point:
- 87 °C
- Boiling point:
- 317.0±22.0 °C(Predicted)
- Density
- 1?+-.0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
Safety
- HS Code
- 2909309090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
H412Harmful to aquatic life with long lasting effects
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P273Avoid release to the environment.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- M304498
- Product name
- 1-(2-Methoxyethoxy)-4-nitrobenzene
- Packaging
- 100mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- M304498
- Product name
- 1-(2-Methoxyethoxy)-4-nitrobenzene
- Packaging
- 500mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- J96335
- Product name
- 1-(2-Methoxyethoxy)-4-nitrobenzene
- Packaging
- 1g
- Price
- $22
- Updated
- 2021/12/16
- Product number
- Z4445
- Product name
- 1-(2-Methoxyethoxy)-4-nitrobenzene
- Packaging
- 1g
- Price
- $29
- Updated
- 2021/12/16
- Product number
- 119927
- Product name
- 1-(2-Methoxyethoxy)-4-nitrobenzene
- Purity
- 95+%
- Packaging
- 1g
- Price
- $78
- Updated
- 2021/12/16
4-NITROPHENYL-2-METHOXYETHYL ETHER Chemical Properties,Usage,Production
Synthesis
100-02-7
6482-24-2
22483-40-5
To a solution of N,N-dimethylformamide (DMF, 10 mL) of 4-nitrophenol (2.78 g, 20 mmol) and 2-bromoethyl methyl ether (3.6 g, 26 mmol) was added anhydrous potassium carbonate (K2CO3, 5.52 g, 40 mmol). The reaction mixture was stirred at 80 °C for 5 hours. Upon completion of the reaction, the mixture was cooled to room temperature and the reaction was subsequently quenched with deionized water (30 mL) and ethyl acetate (EtOAc, 40 mL). The organic and aqueous layers were separated and the aqueous layer was further extracted with ethyl acetate (2 x 25 mL). All organic extracts were combined, washed with saturated sodium chloride solution (brine, 2×20 mL), dried over anhydrous sodium sulfate (Na2SO4), and concentrated under reduced pressure to afford the target product, 4-nitrophenyl-2-methoxyethyl ether (3.9 g, 100% yield) as a yellow solid.
References
[1] Patent: WO2014/130693, 2014, A1. Location in patent: Paragraph 00544; 00546
[2] Patent: WO2015/6754, 2015, A2. Location in patent: Paragraph 00243; 00244
[3] European Journal of Medicinal Chemistry, 1980, vol. 15, # 5, p. 399 - 404
[4] Patent: US2005/277668, 2005, A1. Location in patent: Page/Page column 17
4-NITROPHENYL-2-METHOXYETHYL ETHER Preparation Products And Raw materials
Raw materials
Preparation Products
4-NITROPHENYL-2-METHOXYETHYL ETHER Suppliers
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