6-Nitro-2-(4-Nitrophenyl)Imidazo[1,2-A]Pyridine

Reagent Code: #220144
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CAS Number 118000-57-0

science Other reagents with same CAS 118000-57-0

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Weight 284.23 g/mol
Formula C₁₃H₈N₄O₄
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Storage Room temperature

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Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Plays a role in the development of organic semiconductors for OLEDs due to its electron-deficient structure. Also employed in medicinal chemistry as a building block for nitroaromatic compounds with potential antimicrobial, antiparasitic, and antiviral activity. Its nitro groups allow for further functionalization in multi-step synthesis of bioactive molecules, including those that inhibit microbial enzymes. Additionally, it serves as a fluorescent probe in biological detection systems due to its UV-induced luminescence, aiding in tracking biomolecular reactions in laboratory settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,700.00
inventory 5g
10-20 days ฿8,370.00
inventory 10g
10-20 days ฿16,720.00

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6-Nitro-2-(4-Nitrophenyl)Imidazo[1,2-A]Pyridine
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Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Plays a role in the development of organic semiconductors for OLEDs due to its electron-deficient structure. Also employed in medicinal chemistry as a building block for nitroaromatic compounds with potential antimicrobial, antiparasitic, and antiviral activity. Its nitro groups allow for further functionalization in multi-step synthesis of bioactive molecules, including those that inhibit micr

Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Plays a role in the development of organic semiconductors for OLEDs due to its electron-deficient structure. Also employed in medicinal chemistry as a building block for nitroaromatic compounds with potential antimicrobial, antiparasitic, and antiviral activity. Its nitro groups allow for further functionalization in multi-step synthesis of bioactive molecules, including those that inhibit microbial enzymes. Additionally, it serves as a fluorescent probe in biological detection systems due to its UV-induced luminescence, aiding in tracking biomolecular reactions in laboratory settings.

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