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Structure of 2075-46-9
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4-Nitropyrazole features a nitro group at the para position relative to the pyrazole ring, imparting strong electron-withdrawing character and enhancing reactivity in heterocyclic synthesis. This bench-stable compound serves as a key intermediate in the development of bioactive molecules and functional materials.
4-Nitropyrazole serves as a versatile heterocyclic building block in medicinal chemistry and agrochemical synthesis. The nitro group at the C4 position enables direct electrophilic substitution, facilitates subsequent reduction to an amine for further functionalization, and enhances reactivity in cross-coupling processes. Its bench-stable nature and compatibility with common protecting groups support efficient multi-step synthesis. This compound functions as a key scaffold for constructing bioactive molecules through well-established transformations.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: