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

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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)

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Safety

HS Code: 2909498090

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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.

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N-Bromosuccinimide Price

Apolloscientific

Product number: OR950276
Product name: 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
Purity: 95%
Packaging: 250mg
Price: $269
Updated: 2021/12/16

Apolloscientific

Product number: OR950276
Product name: 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
Purity: 95%
Packaging: 1g
Price: $682
Updated: 2021/12/16

Chemenu

Product number: CM183274
Product name: 1-(4-methoxyphenyl)-2-methylpropan-1-ol
Purity: 95%
Packaging: 1g
Price: $102
Updated: 2021/12/16

Abosyn

Product number: 61-10881
Product name: 1-(4-Methoxyphenyl)-2-methylpropan-1-ol
Purity: 95-98%
Packaging: 1g
Price: $225
Updated: 2021/12/16

Chemenu

Product number: CM183274
Product name: 1-(4-methoxyphenyl)-2-methylpropan-1-ol
Purity: 95%
Packaging: 5g
Price: $281
Updated: 2021/12/16

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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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1-(4-Methoxyphenyl)-2-methylpropan-1-ol Suppliers

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18228-46-1, 1-(4-Methoxyphenyl)-2-methylpropan-1-olRelated Search:

1-(4-Methoxyphenyl)-2-methylpropan-1-ol

1-(p-methoxyphenyl)-2-methylpropan-1-ol

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18228-46-1