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Structure of 70951-96-1
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4-Bromo-5-methyl-3-nitro-1H-pyrazole features a fused heterocyclic core with complementary electron-withdrawing and donor substituents, enabling efficient functionalization in transition metal-catalyzed cross-coupling reactions. The bromine atom serves as a high-reactivity handle for palladium-mediated transformations, while the nitro group enhances electrophilicity at C3. This scaffold demonstrates stability under standard bench conditions and facilitates rapid access to complex nitrogen-containing architectures in medicinal chemistry and materials science applications.
4-Bromo-5-methyl-3-nitro-1H-pyrazole serves as a versatile building block in medicinal chemistry, enabling direct access to substituted pyrazole scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates efficient C–C bond formation under standard Suzuki or Stille conditions, while the nitro and methyl substituents provide orthogonal functional handles for further derivatization. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for high-throughput synthesis and API intermediate 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: