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Structure of 6310-17-4
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2-Bromo-1-(tert-butyl)-4-nitrobenzene features a sterically shielded tert-butyl group and a nitro substituent positioned ortho to the bromine, enabling selective cross-coupling reactions. The electron-deficient aryl bromide integrates efficiently into palladium-catalyzed transformations under standard conditions, delivering complex functionalized arenes with high regiocontrol.
2-Bromo-1-(tert-butyl)-4-nitrobenzene serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki and Stille reactions due to its stable bromide and electron-withdrawing nitro group. The tert-butyl substituent provides steric protection and enhances bench stability, while the ortho-bromo and para-nitro arrangement facilitates selective functionalization. This compound functions effectively in the synthesis of substituted arenes and heterocyclic scaffolds relevant to pharmaceutical 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: