2-((6-Aminobenzo[d]thiazol-2-yl)thio)-N-(2,6-diethylphenyl)acetamide

98%

Reagent Code: #215431
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CAS Number 311762-65-9

science Other reagents with same CAS 311762-65-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.52 g/mol
Formula C₁₉H₂₁N₃OS₂
inventory_2 Storage & Handling
Density 1.30±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in the development of fluorescent probes for bioimaging due to its strong emission properties in the visible range. Its structure allows for selective binding to specific biomolecules, making it useful in detecting enzyme activity or cellular components in live cells. Also investigated as a building block in the synthesis of photosensitive materials for diagnostic assays. Shows potential in optoelectronic applications because of its electron-transport characteristics and stability under light exposure.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿5,930.00
25mg
10-20 days ฿18,690.00
100mg
10-20 days ฿43,990.00
2-((6-Aminobenzo[d]thiazol-2-yl)thio)-N-(2,6-diethylphenyl)acetamide
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Used in the development of fluorescent probes for bioimaging due to its strong emission properties in the visible range. Its structure allows for selective binding to specific biomolecules, making it useful in detecting enzyme activity or cellular components in live cells. Also investigated as a building block in the synthesis of photosensitive materials for diagnostic assays. Shows potential in optoelectronic applications because of its electron-transport characteristics and stability under light exposu

Used in the development of fluorescent probes for bioimaging due to its strong emission properties in the visible range. Its structure allows for selective binding to specific biomolecules, making it useful in detecting enzyme activity or cellular components in live cells. Also investigated as a building block in the synthesis of photosensitive materials for diagnostic assays. Shows potential in optoelectronic applications because of its electron-transport characteristics and stability under light exposure.

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