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Structure of 1350323-81-7
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4-Bromo-5-chloro-1-methyl-1H-pyrazole features a halogenated pyrazole core with complementary bromo and chloro substituents at adjacent positions, enabling selective coupling in cross-coupling reactions. The methyl group enhances solubility and stabilizes the heterocyclic ring under standard conditions. This scaffold serves as a key building block for bioactive molecules in medicinal chemistry and agrochemical development.
4-Bromo-5-chloro-1-methyl-1H-pyrazole serves as a versatile heterocyclic building block in medicinal chemistry and agrochemical synthesis. Its complementary halogenation pattern enables sequential cross-coupling reactions, while the methyl group provides a handle for further functionalization. The compound exhibits good bench stability and facilitates efficient Pd-catalyzed transformations, making it well-suited for constructing complex molecular architectures in multi-step synthetic sequences.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: