6-(Trifluoromethyl)-2(3H)-benzothiazolethione

≥95%

Reagent Code: #241564
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CAS Number 401567-22-4

science Other reagents with same CAS 401567-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.250 g/mol
Formula C₈H₄F₃NS₂
inventory_2 Storage & Handling
Storage 2-8℃, dry, sealed

description Product Description

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its strong electron-withdrawing trifluoromethyl group and sulfur-containing heterocyclic structure. It also serves in the development of agrochemicals, particularly as a building block for fungicides and herbicides, where the thione functionality enhances binding to target enzymes. Additionally, it has been investigated for use in medicinal chemistry, especially in the design of inhibitors targeting cysteine proteases, owing to its ability to interact with active-site thiols. Its unique structure supports applications in materials science, including organic semiconductors and sensors, where stability and electronic properties are critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,330.00
inventory 1g
10-20 days ฿12,550.00
inventory 5g
10-20 days ฿38,460.00
6-(Trifluoromethyl)-2(3H)-benzothiazolethione
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Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its strong electron-withdrawing trifluoromethyl group and sulfur-containing heterocyclic structure. It also serves in the development of agrochemicals, particularly as a building block for fungicides and herbicides, where the thione functionality enhances binding to target enzymes. Additionally, it has been investigated for use in medicinal chemistry, especially in the design of inhibitors targeting cysteine prote

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its strong electron-withdrawing trifluoromethyl group and sulfur-containing heterocyclic structure. It also serves in the development of agrochemicals, particularly as a building block for fungicides and herbicides, where the thione functionality enhances binding to target enzymes. Additionally, it has been investigated for use in medicinal chemistry, especially in the design of inhibitors targeting cysteine proteases, owing to its ability to interact with active-site thiols. Its unique structure supports applications in materials science, including organic semiconductors and sensors, where stability and electronic properties are critical.

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