1-(4-Methoxyphenyl)-2-methylpropan-1-ol
- Product Name
- 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
- CAS No.
- 18228-46-1
- Chemical Name
- 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
- Synonyms
- 1-(p-methoxyphenyl)-2-methylpropan-1-ol;1-(4-Methoxyphenyl)-2-methylpropan-1-ol;Benzenemethanol, 4-methoxy-α-(1-methylethyl)-
- CBNumber
- CB92743928
- Molecular Formula
- C11H16O2
- Formula Weight
- 180.24
- MOL File
- 18228-46-1.mol
1-(4-Methoxyphenyl)-2-methylpropan-1-ol Property
- Boiling point:
- 150 °C(Press: 14 Torr)
- Density
- 1.0453 g/cm3(Temp: 0 °C)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 14.36±0.20(Predicted)
Safety
- HS Code
- 2909498090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H227Combustible liquid
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
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
- OR950276
- Product name
- 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
- Purity
- 95%
- Packaging
- 250mg
- Price
- $269
- Updated
- 2021/12/16
- Product number
- OR950276
- Product name
- 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
- Purity
- 95%
- Packaging
- 1g
- Price
- $682
- Updated
- 2021/12/16
- Product number
- CM183274
- Product name
- 1-(4-methoxyphenyl)-2-methylpropan-1-ol
- Purity
- 95%
- Packaging
- 1g
- Price
- $102
- Updated
- 2021/12/16
- Product number
- 61-10881
- Product name
- 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
- Purity
- 95-98%
- Packaging
- 1g
- Price
- $225
- Updated
- 2021/12/16
- Product number
- CM183274
- Product name
- 1-(4-methoxyphenyl)-2-methylpropan-1-ol
- Purity
- 95%
- Packaging
- 5g
- Price
- $281
- Updated
- 2021/12/16
1-(4-Methoxyphenyl)-2-methylpropan-1-ol Chemical Properties,Usage,Production
Synthesis
1068-55-9
123-11-5
18228-46-1
A solution was prepared by dissolving 1.5 mL of 4-methoxybenzaldehyde in 10 mL of toluene at 8 °C. This solution was slowly added dropwise to 7.4 mL of 2M isopropylmagnesium chloride solution. After the dropwise addition was completed, the reaction mixture was gradually warmed to room temperature and stirred continuously for 1 hour. Upon completion of the reaction, the reaction was terminated by addition of a half-saturated aqueous ammonium chloride solution. Subsequently, the organic and aqueous phases were separated and the aqueous phase was extracted with toluene. All organic phases were combined and washed with an aqueous solution of half-saturated and ammonium chloride, followed by drying with magnesium sulfate. The solvent was removed under reduced pressure and the resulting product was used for subsequent reactions without further purification. The final yield was 2.12 g in 95% of the theoretical value. The product was analyzed by HPLC (Method 1) with a retention time of 3.22 min.
References
[1] Patent: US2011/269737, 2011, A1. Location in patent: Page/Page column 63
[2] Australian Journal of Chemistry, 1986, vol. 39, # 12, p. 2095 - 2110
[3] Patent: US2597446, 1949,
1-(4-Methoxyphenyl)-2-methylpropan-1-ol Preparation Products And Raw materials
Raw materials
Preparation Products
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