N-(6-nitrobenzothiazol-2-yl)cyclopentanecarboxamide

Reagent Code: #216091
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CAS Number 545437-45-4

science Other reagents with same CAS 545437-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.331 g/mol
Formula C₁₃H₁₃N₃O₃S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Exhibits strong binding affinity in biochemical assays, making it suitable for development in fluorescent labeling of proteins and cellular imaging. Also investigated for its potential in agrochemical formulations due to its stability under UV light and moderate thermal conditions. Shows promise in sensor technologies for detecting metal ions in environmental samples owing to its electron-withdrawing nitro group and rigid benzothiazole framework.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿22,800.00
N-(6-nitrobenzothiazol-2-yl)cyclopentanecarboxamide
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Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Exhibits strong binding affinity in biochemical assays, making it suitable for development in fluorescent labeling of proteins and cellular imaging. Also investigated for its potential in agrochemical formulations due to its stability under UV light and moderate thermal conditions. Shows promise in sensor technologies for detecting metal ions in environmental samples owing to its electron-withd

Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Exhibits strong binding affinity in biochemical assays, making it suitable for development in fluorescent labeling of proteins and cellular imaging. Also investigated for its potential in agrochemical formulations due to its stability under UV light and moderate thermal conditions. Shows promise in sensor technologies for detecting metal ions in environmental samples owing to its electron-withdrawing nitro group and rigid benzothiazole framework.

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