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2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester

Product Name
2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester
CAS No.
6274-50-6
Chemical Name
2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester
Synonyms
Methyl 2-(4-Methoxyphenyl)-2-Methylpropanoate;2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester;Benzeneacetic acid, 4-methoxy-α,α-dimethyl-, methyl ester
CBNumber
CB02550479
Molecular Formula
C12H16O3
Formula Weight
208.25
MOL File
6274-50-6.mol
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2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester Property

storage temp. 
Sealed in dry,Room Temperature
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0392882
Product name
METHYL-2-(4-METHOXYPHENYL)-2-METHYLPROPANOATE
Purity
95.00%
Packaging
5MG
Price
$498.73
Updated
2021/12/16
Matrix Scientific
Product number
126898
Product name
Methyl2-(4-methoxyphenyl)-2-methylpropanoate
Purity
>95%
Packaging
1g
Price
$694
Updated
2021/12/16
Matrix Scientific
Product number
126898
Product name
Methyl2-(4-methoxyphenyl)-2-methylpropanoate
Purity
>95%
Packaging
5g
Price
$2080
Updated
2021/12/16
Chemcia Scientific
Product number
CC00-1136
Product name
2-(4-Methoxy-phenyl)-2-methyl-propionic acid methyl ester
Purity
>97%
Packaging
5G
Price
$875
Updated
2021/12/16
Abosyn
Product number
61-10080
Product name
Methyl2-(4-methoxyphenyl)-2-methylpropanoate
Purity
95-98%
Packaging
1g
Price
$1040
Updated
2021/12/16
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2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester Chemical Properties,Usage,Production

Synthesis

23786-14-3

74-88-4

6274-50-6

Methyl iodomethane (23.64 g, 166.5 mmol) was added slowly and dropwise to a tetrahydrofuran (THF, 100 mL) solution of methyl 2-(4-methoxyphenyl)acetate (10.0 g, 55.49 mmol) at -78 °C. Subsequently, potassium tert-butoxide (KOt-Bu, 18.68 g, 166.5 mmol) was added in batches over 30 min, keeping the reaction mixture stirred at -78 °C for 1 h. The reaction was then brought to room temperature and continued to be stirred for 1 h. The reaction was completed by the addition of potassium tert-butoxide (KOt-Bu, 18.68 g, 166.5 mmol). Upon completion of the reaction, the reaction was quenched by the addition of water (25 mL) and extracted with ethyl acetate (EtOAc, 2 x 250 mL). The organic layers were combined, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give methyl 2-(4-methoxyphenyl)-2-methylpropionate (10.46 g, 91% yield).

References

[1] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 87
[2] Patent: WO2013/19635, 2013, A1. Location in patent: Page/Page column 55
[3] Helvetica Chimica Acta, 1971, vol. 54, p. 868 - 897
[4] Biomedical mass spectrometry, 1976, vol. 3, # 6, p. 316 - 328
[5] Patent: US5776951, 1998, A

2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester Preparation Products And Raw materials

Raw materials

Preparation Products

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2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester Suppliers

Alfa Chemistry
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+1-5166625404;
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1-516-927-0118
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Info@alfa-chemistry.com
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United States
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20405
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Aladdin Scientific
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Email
tp@aladdinsci.com
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United States
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52923
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58
Synthonix Inc
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info@synthonix.com
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United States
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6872
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Combi-Blocks Inc.
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sales@combi-blocks.com
Country
United States
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6618
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Matrix Scientific
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Email
sales@matrixscientific.com
Country
United States
ProdList
6632
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6274-50-6, 2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylesterRelated Search:


  • 2-(4-Methoxy-phenyl)-2-Methyl-propionicacidMethylester
  • Methyl 2-(4-Methoxyphenyl)-2-Methylpropanoate
  • Benzeneacetic acid, 4-methoxy-α,α-dimethyl-, methyl ester
  • 6274-50-6