(3aS,6R,7aR)-8,8-Dimethyl-1-((trifluoromethyl)thio)hexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide

97%

Reagent Code: #236811
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CAS Number 2094737-51-4

science Other reagents with same CAS 2094737-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.3755 g/mol
Formula C₁₁H₁₆F₃NO₂S₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of neuroprotective agents and anti-inflammatory drugs. Its unique bridged ring structure and trifluoromethylthio group enhance metabolic stability and bioavailability in target molecules. Employed in research settings for structure-activity relationship studies due to its rigid scaffold and electron-withdrawing sulfone functionality. Also explored in agrochemical research for designing novel bioactive molecules with improved environmental stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,080.00
inventory 250mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿5,810.00
inventory 5g
10-20 days ฿20,320.00

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(3aS,6R,7aR)-8,8-Dimethyl-1-((trifluoromethyl)thio)hexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of neuroprotective agents and anti-inflammatory drugs. Its unique bridged ring structure and trifluoromethylthio group enhance metabolic stability and bioavailability in target molecules. Employed in research settings for structure-activity relationship studies due to its rigid scaffold and electron-withdrawing sulfone functionality. Also explored in agrochemical research for designing novel bioactive mo

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of neuroprotective agents and anti-inflammatory drugs. Its unique bridged ring structure and trifluoromethylthio group enhance metabolic stability and bioavailability in target molecules. Employed in research settings for structure-activity relationship studies due to its rigid scaffold and electron-withdrawing sulfone functionality. Also explored in agrochemical research for designing novel bioactive molecules with improved environmental stability.

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