3-(2,5,5-Trimethyl-1,3-dioxan-2-yl)thiophene-2-sulfonamide

95%

Reagent Code: #238256
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CAS Number 138890-87-6

science Other reagents with same CAS 138890-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.39 g/mol
Formula C₁₁H₁₇NO₄S₂
badge Registry Numbers
MDL Number MFCD23135557
thermostat Physical Properties
Boiling Point 442.1±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.278 g/cm3
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceutical agents targeting central nervous system disorders. Its sulfonamide group enhances binding affinity to certain enzyme targets, making it valuable in medicinal chemistry for designing inhibitors. Also employed in agrochemical research for creating novel pesticides with improved selectivity and lower environmental impact. The dioxane-thiophene scaffold contributes to metabolic stability, which is beneficial in optimizing drug candidates for better pharmacokinetic profiles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,550.00
inventory 1g
10-20 days ฿48,360.00
3-(2,5,5-Trimethyl-1,3-dioxan-2-yl)thiophene-2-sulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceutical agents targeting central nervous system disorders. Its sulfonamide group enhances binding affinity to certain enzyme targets, making it valuable in medicinal chemistry for designing inhibitors. Also employed in agrochemical research for creating novel pesticides with improved selectivity and lower environmental impact. The dioxane-thiophene scaffold contributes to metabolic stabili

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceutical agents targeting central nervous system disorders. Its sulfonamide group enhances binding affinity to certain enzyme targets, making it valuable in medicinal chemistry for designing inhibitors. Also employed in agrochemical research for creating novel pesticides with improved selectivity and lower environmental impact. The dioxane-thiophene scaffold contributes to metabolic stability, which is beneficial in optimizing drug candidates for better pharmacokinetic profiles.

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