2-Methoxyphenylsulfonylethanol

≥97%

Reagent Code: #213390
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CAS Number 75259-57-3

science Other reagents with same CAS 75259-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.26 g/mol
Formula C₉H₁₂O₄S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its sulfonylethanol structure allows it to act as a building block for constructing more complex molecules, especially in reactions involving functional group transformations or ring formation. It is also employed in the development of sulfone-based bioactive compounds due to the stability and reactivity of the sulfone moiety. Its methoxyphenyl group can aid in directing electrophilic substitutions or serve as a protecting group in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿29,600.00

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2-Methoxyphenylsulfonylethanol
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its sulfonylethanol structure allows it to act as a building block for constructing more complex molecules, especially in reactions involving functional group transformations or ring formation. It is also employed in the development of sulfone-based bioactive compounds due to the stability and reactivity of the sulfone moiety. Its methoxyphenyl group can aid in directing electrophilic subst

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its sulfonylethanol structure allows it to act as a building block for constructing more complex molecules, especially in reactions involving functional group transformations or ring formation. It is also employed in the development of sulfone-based bioactive compounds due to the stability and reactivity of the sulfone moiety. Its methoxyphenyl group can aid in directing electrophilic substitutions or serve as a protecting group in multi-step syntheses.

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