S-methyl-s-(3-methylphenyl) sulfoximine

95%

Reagent Code: #236228
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CAS Number 22132-98-5

science Other reagents with same CAS 22132-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.24 g/mol
Formula C₈H₁₁NOS
badge Registry Numbers
MDL Number MFCD09878524
thermostat Physical Properties
Boiling Point 265.5±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of certain pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a chiral building block in asymmetric synthesis, enabling the formation of structurally complex molecules with high enantioselectivity. Its sulfoximine moiety enhances binding affinity and metabolic stability in drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,390.00
inventory 250mg
10-20 days ฿19,140.00
inventory 1g
10-20 days ฿49,770.00

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S-methyl-s-(3-methylphenyl) sulfoximine
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Used as a key intermediate in the synthesis of certain pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a chiral building block in asymmetric synthesis, enabling the formation of structurally complex molecules with high enantioselectivity. Its sulfoximine moiety enhances binding affinity and metabolic stability in drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profile.<

Used as a key intermediate in the synthesis of certain pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a chiral building block in asymmetric synthesis, enabling the formation of structurally complex molecules with high enantioselectivity. Its sulfoximine moiety enhances binding affinity and metabolic stability in drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profile.

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