Methyl 4-Methyl-3-(methylsulfonyl)benzoate

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Reagent Code: #172215
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CAS Number 906816-32-8

science Other reagents with same CAS 906816-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.26 g/mol
Formula C₁₀H₁₂O₄S
badge Registry Numbers
MDL Number MFCD22586702
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in the preparation of sulfone-containing bioactive molecules, where the methylsulfonyl group contributes to enhanced binding affinity and selectivity. Additionally, it serves as a building block in agrochemical research for designing novel pesticides with improved environmental profiles.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,190.00
inventory 1g
10-20 days ฿5,660.00
inventory 5g
10-20 days ฿18,310.00
Methyl 4-Methyl-3-(methylsulfonyl)benzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in the preparation of sulfone-containing bioactive molecules, where the methylsulfonyl group contributes to enhanced binding affinity and selectivity. Additionally, it serves as a building block in agrochemical

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in the preparation of sulfone-containing bioactive molecules, where the methylsulfonyl group contributes to enhanced binding affinity and selectivity. Additionally, it serves as a building block in agrochemical research for designing novel pesticides with improved environmental profiles.

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