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Structure of 536759-91-8
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Ethyl 1-(4-methoxyphenyl)-6-(4-nitrophenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate features a fused pyrazolopyridine core with distinct electron-rich and electron-deficient aryl substituents. This scaffold integrates a methoxy-activated phenyl group at C1 and a nitro-bearing phenyl at C6, enabling precise tuning of reactivity in transition-metal-catalyzed transformations. The ester functionality supports downstream derivatization, while the saturated ring system enhances solubility and stability under standard bench conditions.
Ethyl 1-(4-methoxyphenyl)-6-(4-nitrophenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate serves as a versatile scaffold for the synthesis of bioactive heterocycles, enabling efficient access to pyrazolopyridine-based intermediates. Its functional group array—comprising a nitro group, methoxy aryl, and ester—supports diverse transformations including reduction, nucleophilic substitution, and palladium-catalyzed coupling. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: