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Structure of 95162-14-4
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4-Bromo-1-tritylpyrazole serves as a protected pyrazole synthon for late-stage functionalization in medicinal chemistry. The trityl group provides robust protection of the nitrogen, enabling selective transformations under mild conditions. This derivative combines enhanced stability with high reactivity at the bromine site, facilitating efficient cross-coupling and diversification in complex molecule synthesis.
4-Bromo-1-tritylpyrazole serves as a versatile building block for the synthesis of functionalized pyrazole derivatives, enabling efficient late-stage diversification in medicinal chemistry. The trityl group provides robust protection for the pyrazole nitrogen, ensuring stability during multistep syntheses and facilitating straightforward deprotection under mild acidic conditions. Its bromine substituent supports diverse cross-coupling reactions, including Pd-catalyzed Suzuki and Negishi transformations, making it ideal for constructing complex heterocyclic scaffolds with high functional group tolerance and excellent purification profiles.
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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: