2-Nitrophenyl selenocyanate

97%

Reagent Code: #219740
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CAS Number 51694-22-5

science Other reagents with same CAS 51694-22-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.08 g/mol
Formula C₇H₄N₂O₂Se
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MDL Number MFCD00043146
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in the preparation of selenated compounds. It serves as a source of selenium in the formation of carbon–selenium bonds, which are valuable in the development of functional materials and bioactive molecules. Its nitrophenyl group enhances reactivity and can act as a chromophore, making it useful in spectroscopic studies. Applied in the synthesis of selenium-containing heterocycles and in radical reactions where controlled selenium transfer is required. Also explored in the modification of biomolecules for research purposes due to selenium’s unique redox properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,290.00
2-Nitrophenyl selenocyanate
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Used as a reagent in organic synthesis, particularly in the preparation of selenated compounds. It serves as a source of selenium in the formation of carbon–selenium bonds, which are valuable in the development of functional materials and bioactive molecules. Its nitrophenyl group enhances reactivity and can act as a chromophore, making it useful in spectroscopic studies. Applied in the synthesis of selenium-containing heterocycles and in radical reactions where controlled selenium transfer is required.

Used as a reagent in organic synthesis, particularly in the preparation of selenated compounds. It serves as a source of selenium in the formation of carbon–selenium bonds, which are valuable in the development of functional materials and bioactive molecules. Its nitrophenyl group enhances reactivity and can act as a chromophore, making it useful in spectroscopic studies. Applied in the synthesis of selenium-containing heterocycles and in radical reactions where controlled selenium transfer is required. Also explored in the modification of biomolecules for research purposes due to selenium’s unique redox properties.

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