6-nitro-2-((trifluoromethyl)thio)benzo[d]isothiazol-3(2H)-one 1,1-dioxide

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Reagent Code: #196710
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CAS Number 1857384-53-2

science Other reagents with same CAS 1857384-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 328.250 g/mol
Formula C₈H₃F₃N₂O₅S₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antimicrobial and anti-inflammatory properties. Its structure, featuring a nitro group and a (trifluoromethyl)thio substituent, supports use in agrochemical research, especially in creating novel pesticides and herbicides, as these groups enhance bioavailability and stability. Also employed in material science for designing fluorescent probes and sensors, leveraging its electron-withdrawing groups and rigid aromatic framework for optical applications.

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inventory 1g
10-20 days ฿54,750.00

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6-nitro-2-((trifluoromethyl)thio)benzo[d]isothiazol-3(2H)-one 1,1-dioxide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antimicrobial and anti-inflammatory properties. Its structure, featuring a nitro group and a (trifluoromethyl)thio substituent, supports use in agrochemical research, especially in creating novel pesticides and herbicides, as these groups enhance bioavailability and stability. Also employed in material science for designing fluorescent probes and sensors, leveraging

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antimicrobial and anti-inflammatory properties. Its structure, featuring a nitro group and a (trifluoromethyl)thio substituent, supports use in agrochemical research, especially in creating novel pesticides and herbicides, as these groups enhance bioavailability and stability. Also employed in material science for designing fluorescent probes and sensors, leveraging its electron-withdrawing groups and rigid aromatic framework for optical applications.

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