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2-PHENYLETHYLMETHANESULPHONATE

Product Name
2-PHENYLETHYLMETHANESULPHONATE
CAS No.
20020-27-3
Chemical Name
2-PHENYLETHYLMETHANESULPHONATE
Synonyms
3-phenylpropane-1-sulfonate;2-PHENYLETHYLMETHANESULPHONATE;2-phenylethyl methanesulfonate;Methanesulfonic acid, 2-phenylethyl ester
CBNumber
CB11445065
Molecular Formula
C9H12O3S
Formula Weight
200.25
MOL File
20020-27-3.mol
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2-PHENYLETHYLMETHANESULPHONATE Property

Boiling point:
358.1±21.0 °C(Predicted)
Density 
1.205±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Abosyn
Product number
61-10142
Product name
Phenethylmethanesulfonate
Purity
95-98%
Packaging
1g
Price
$225
Updated
2021/12/16
Alichem
Product number
20020273
Product name
Phenethylmethanesulfonate
Packaging
5g
Price
$352.8
Updated
2021/12/16
Crysdot
Product number
CD12098755
Product name
Phenethylmethanesulfonate
Purity
98%
Packaging
5g
Price
$356
Updated
2021/12/16
Crysdot
Product number
CD12098755
Product name
Phenethylmethanesulfonate
Purity
98%
Packaging
10g
Price
$594
Updated
2021/12/16
Alichem
Product number
20020273
Product name
Phenethylmethanesulfonate
Packaging
10g
Price
$594
Updated
2021/12/16
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2-PHENYLETHYLMETHANESULPHONATE Chemical Properties,Usage,Production

Synthesis

60-12-8

124-63-0

20020-27-3

GENERAL METHOD: Phenylethanol (2.14 mmol) was dissolved in anhydrous dichloromethane (6 mL) with triethylamine (0.36 mL, 2.59 mmol) under nitrogen protection and cooled to 0 °C. Subsequently, methanesulfonyl chloride (0.18 mL, 2.31 mmol) was slowly added dropwise and the reaction temperature was maintained at 0 °C for 1 hour. After that, the reaction mixture was gradually warmed up to room temperature and stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane (3 x 30 mL). The organic phases were combined and washed sequentially with 10% aqueous hydrochloric acid and saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure, and the resulting crude product was purified by silica gel column chromatography, sequentially using dichloromethane and chloroform as eluents, to obtain the target product, phenethyl methanesulfonate, the structure of which was confirmed by the method described in the Supplementary Material.

References

[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 7, p. 3000 - 3012
[2] Synthetic Communications, 2011, vol. 41, # 5, p. 748 - 753
[3] Journal of Organic Chemistry, 1993, vol. 58, # 1, p. 272 - 274
[4] Tetrahedron, 2016, vol. 72, # 49, p. 8022 - 8030
[5] Journal of Medicinal Chemistry, 1990, vol. 33, # 10, p. 2807 - 2813

2-PHENYLETHYLMETHANESULPHONATE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-PHENYLETHYLMETHANESULPHONATE Suppliers

A.J Chemicals
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sales@ajchem.in
Country
India
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