6-Nitrobenzo[d]isothiazol-3(2H)-one 1,1-dioxide

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Reagent Code: #217319
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CAS Number 22952-24-5

science Other reagents with same CAS 22952-24-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.18 g/mol
Formula C₇H₄N₂O₅S
thermostat Physical Properties
Melting Point 205-207°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of heterocyclic systems with potential antimicrobial, anti-inflammatory, or insecticidal properties. Commonly employed in research settings for constructing fused isothiazole derivatives that show promise in drug discovery programs. Also utilized in the preparation of fluorescent probes and dyes due to its electron-withdrawing nitro group and stable sulfonamide moiety, enabling applications in bioimaging and molecular labeling.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,260.00
inventory 5g
10-20 days ฿4,530.00
inventory 25g
10-20 days ฿15,850.00
inventory 100g
10-20 days ฿37,360.00
inventory 500g
10-20 days ฿161,500.00

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6-Nitrobenzo[d]isothiazol-3(2H)-one 1,1-dioxide
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of heterocyclic systems with potential antimicrobial, anti-inflammatory, or insecticidal properties. Commonly employed in research settings for constructing fused isothiazole derivatives that show promise in drug discovery programs. Also utilized in the preparation of fluorescent probes and dyes due to its electron-withdrawing nitro group

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of heterocyclic systems with potential antimicrobial, anti-inflammatory, or insecticidal properties. Commonly employed in research settings for constructing fused isothiazole derivatives that show promise in drug discovery programs. Also utilized in the preparation of fluorescent probes and dyes due to its electron-withdrawing nitro group and stable sulfonamide moiety, enabling applications in bioimaging and molecular labeling.

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