S-(4-fluorophenyl)-S-Methyl-SulfoxiMine

95%

Reagent Code: #236202
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CAS Number 635311-89-6

science Other reagents with same CAS 635311-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.21 g/mol
Formula C₇H₈FNOS
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfoximine group enhances metabolic stability and binding selectivity, making it valuable in drug design. Commonly employed in the development of kinase inhibitors and protease inhibitors due to its ability to mimic transition states in enzymatic reactions. Also utilized in agrochemicals for improving the potency and environmental stability of certain pesticides. Its fluorinated aromatic moiety contributes to improved lipophilicity and bioavailability in final active ingredients.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,550.00
inventory 250mg
10-20 days ฿8,900.00
inventory 1g
10-20 days ฿24,000.00

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S-(4-fluorophenyl)-S-Methyl-SulfoxiMine
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Used as a key chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfoximine group enhances metabolic stability and binding selectivity, making it valuable in drug design. Commonly employed in the development of kinase inhibitors and protease inhibitors due to its ability to mimic transition states in enzymatic reactions. Also utilized in agrochemicals for improving the potency and environmental stabilit

Used as a key chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfoximine group enhances metabolic stability and binding selectivity, making it valuable in drug design. Commonly employed in the development of kinase inhibitors and protease inhibitors due to its ability to mimic transition states in enzymatic reactions. Also utilized in agrochemicals for improving the potency and environmental stability of certain pesticides. Its fluorinated aromatic moiety contributes to improved lipophilicity and bioavailability in final active ingredients.

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