5-Nitrobenzo[c][1,2,5]thiadiazole

95%

Reagent Code: #218966
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CAS Number 16252-88-3

science Other reagents with same CAS 16252-88-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.17 g/mol
Formula C₆H₃N₃O₂S
badge Registry Numbers
MDL Number MFCD00114840
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a fluorescent probe in bioimaging due to its strong emission upon binding to specific biomolecules. It is also employed in the development of sensors for detecting nitroreductase enzymes, which are overexpressed in hypoxic cancer cells, making it valuable in cancer research. Additionally, it serves as a building block in the synthesis of organic semiconductors and luminescent materials for optoelectronic devices. Its electron-deficient nature allows for use in charge-transfer complexes and as a component in high-energy materials.

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Test Parameter Specification
Appearance Brown Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,140.00
inventory 250mg
10-20 days ฿24,070.00
inventory 1g
10-20 days ฿65,080.00
5-Nitrobenzo[c][1,2,5]thiadiazole
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Used as a fluorescent probe in bioimaging due to its strong emission upon binding to specific biomolecules. It is also employed in the development of sensors for detecting nitroreductase enzymes, which are overexpressed in hypoxic cancer cells, making it valuable in cancer research. Additionally, it serves as a building block in the synthesis of organic semiconductors and luminescent materials for optoelectronic devices. Its electron-deficient nature allows for use in charge-transfer complexes and as a c

Used as a fluorescent probe in bioimaging due to its strong emission upon binding to specific biomolecules. It is also employed in the development of sensors for detecting nitroreductase enzymes, which are overexpressed in hypoxic cancer cells, making it valuable in cancer research. Additionally, it serves as a building block in the synthesis of organic semiconductors and luminescent materials for optoelectronic devices. Its electron-deficient nature allows for use in charge-transfer complexes and as a component in high-energy materials.

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