S-(trifluoromethyl) 2-iodobenzothioate

97%

Reagent Code: #236465
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CAS Number 2376271-53-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.085 g/mol
Formula C₈H₄F₃IOS
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a key reagent in organic synthesis, particularly in transition-metal-catalyzed cross-coupling reactions. It serves as a trifluoromethylthiolating agent, enabling the introduction of the SCF₃ group into organic molecules, which is valuable in pharmaceutical and agrochemical development due to the group’s high lipophilicity and metabolic stability. Commonly employed in the preparation of bioactive compounds and functional materials where enhanced membrane permeability and electron-withdrawing properties are required. Its iodine moiety allows further functionalization via coupling reactions, making it a versatile building block in medicinal chemistry and late-stage diversification of complex molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,320.00
S-(trifluoromethyl) 2-iodobenzothioate
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Used as a key reagent in organic synthesis, particularly in transition-metal-catalyzed cross-coupling reactions. It serves as a trifluoromethylthiolating agent, enabling the introduction of the SCF₃ group into organic molecules, which is valuable in pharmaceutical and agrochemical development due to the group’s high lipophilicity and metabolic stability. Commonly employed in the preparation of bioactive compounds and functional materials where enhanced membrane permeability and electron-withdrawing prope

Used as a key reagent in organic synthesis, particularly in transition-metal-catalyzed cross-coupling reactions. It serves as a trifluoromethylthiolating agent, enabling the introduction of the SCF₃ group into organic molecules, which is valuable in pharmaceutical and agrochemical development due to the group’s high lipophilicity and metabolic stability. Commonly employed in the preparation of bioactive compounds and functional materials where enhanced membrane permeability and electron-withdrawing properties are required. Its iodine moiety allows further functionalization via coupling reactions, making it a versatile building block in medicinal chemistry and late-stage diversification of complex molecules.

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