2-(Allylsulfonyl)-4-methylpyridine

≥98%(GC&T)

Reagent Code: #137286
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CAS Number 2249891-89-0

science Other reagents with same CAS 2249891-89-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.25 g/mol
Formula C₉H₁₁NO₂S
thermostat Physical Properties
Melting Point 116 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of selective enzyme inhibitors. Its structure allows for facile modification in heterocyclic chemistry, making it valuable in creating bioactive molecules. Commonly employed in the preparation of sulfone-containing pyridine derivatives, which show activity in neurological and anti-inflammatory research. Also utilized in agrochemicals for designing novel pesticides with improved metabolic stability. Its allyl sulfonyl group enables efficient cross-coupling reactions, enhancing its utility in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,050.00

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2-(Allylsulfonyl)-4-methylpyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of selective enzyme inhibitors. Its structure allows for facile modification in heterocyclic chemistry, making it valuable in creating bioactive molecules. Commonly employed in the preparation of sulfone-containing pyridine derivatives, which show activity in neurological and anti-inflammatory research. Also utilized in agrochemicals for designing novel pesticides with improved metabolic stability. Its allyl s

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of selective enzyme inhibitors. Its structure allows for facile modification in heterocyclic chemistry, making it valuable in creating bioactive molecules. Commonly employed in the preparation of sulfone-containing pyridine derivatives, which show activity in neurological and anti-inflammatory research. Also utilized in agrochemicals for designing novel pesticides with improved metabolic stability. Its allyl sulfonyl group enables efficient cross-coupling reactions, enhancing its utility in medicinal chemistry and process development.

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