2-(benzylthio)-4-(trifluoromethyl)pyridine

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Reagent Code: #142405
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CAS Number 1393576-27-6

science Other reagents with same CAS 1393576-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.29 g/mol
Formula C₁₃H₁₀F₃NS
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antifungal agents. Its structure supports the creation of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of both benzylthio and trifluoromethyl groups, which enhance metabolic stability and membrane permeability. Also utilized in agrochemical research for designing new crop protection agents with improved efficacy and environmental profiles.

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Test Parameter Specification
Appearance white solid
Purity 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,540.00
inventory 250mg
10-20 days ฿8,640.00

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2-(benzylthio)-4-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antifungal agents. Its structure supports the creation of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of both benzylthio and trifluoromethyl groups, which enhance metabolic stability and membrane permeability. Also utilized in agrochemical research for designin

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antifungal agents. Its structure supports the creation of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of both benzylthio and trifluoromethyl groups, which enhance metabolic stability and membrane permeability. Also utilized in agrochemical research for designing new crop protection agents with improved efficacy and environmental profiles.

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