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Structure of 13745-59-0
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3-Bromo-1,4-dimethyl-1H-pyrazole features a brominated pyrazole core with methyl substituents at the 1- and 4-positions, offering enhanced stability and reactivity in cross-coupling transformations. This bench-stable heterocycle integrates readily into medicinal chemistry libraries, serving as a key scaffold for bioactive molecule synthesis.
3-Bromo-1,4-dimethyl-1H-pyrazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable halogen functionality. The methyl groups at C1 and C4 enhance solubility and provide steric protection, improving bench stability and simplifying purification. This compound functions effectively in Suzuki-Miyaura and Stille couplings, facilitating the construction of complex heterocyclic scaffolds common in drug discovery.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: