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Structure of 2088840-42-8
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2-(4-Bromo-1H-pyrazol-1-yl)-2-methylpropanenitrile features a sterically hindered nitrile group flanked by a brominated pyrazole ring, enabling direct integration into cross-coupling reactions. The electron-deficient pyrazole moiety enhances reactivity in palladium-catalyzed transformations, while the tert-butyl-like structure confers bench stability and ease of handling under standard conditions.
2-(4-Bromo-1H-pyrazol-1-yl)-2-methylpropanenitrile serves as a versatile building block for constructing pyrazole-based scaffolds in medicinal chemistry and materials science. The nitrile group enables downstream functionalization via hydrolysis or nucleophilic addition, while the bromo substituent supports palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. Its tert-butyl-like steric profile enhances bench stability and simplifies purification, making it well-suited for scalable synthesis and modular library 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: