(S)-S-Methyl-S-phenylsulfoximine

97%

Reagent Code: #237469
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CAS Number 33903-50-3

science Other reagents with same CAS 33903-50-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.22 g/mol
Formula C₇H₉NOS
badge Registry Numbers
MDL Number MFCD00151461
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in the preparation of sulfoximine-containing pharmaceuticals. Its stereochemical stability and ability to direct enantioselective transformations make it valuable in drug development. Commonly employed in the synthesis of bioactive molecules where sulfur-containing motifs are required for activity. Also utilized in agrochemical research for designing herbicides and fungicides with improved selectivity. Shows utility in catalysis, serving as a ligand precursor in transition metal-catalyzed reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,560.00
inventory 250mg
10-20 days ฿14,280.00
inventory 1g
10-20 days ฿42,850.00
(S)-S-Methyl-S-phenylsulfoximine
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Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in the preparation of sulfoximine-containing pharmaceuticals. Its stereochemical stability and ability to direct enantioselective transformations make it valuable in drug development. Commonly employed in the synthesis of bioactive molecules where sulfur-containing motifs are required for activity. Also utilized in agrochemical research for designing herbicides and fungicides with improved selectivity. Shows utility in ca

Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in the preparation of sulfoximine-containing pharmaceuticals. Its stereochemical stability and ability to direct enantioselective transformations make it valuable in drug development. Commonly employed in the synthesis of bioactive molecules where sulfur-containing motifs are required for activity. Also utilized in agrochemical research for designing herbicides and fungicides with improved selectivity. Shows utility in catalysis, serving as a ligand precursor in transition metal-catalyzed reactions.

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