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Structure of 142356-35-2
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tert-Butyl (8-bromooctyl)carbamate delivers a brominated alkyl chain tethered to a stable carbamate protecting group, enabling direct functionalization in late-stage synthesis. This bench-stable derivative facilitates efficient coupling reactions and selective transformations under standard conditions.
tert-Butyl (8-bromooctyl)carbamate serves as a versatile protecting group for primary amines, enabling efficient synthesis of aminoalkyl building blocks. The bromide functionality facilitates subsequent palladium-catalyzed cross-coupling reactions, while the tert-butyl carbamate moiety offers excellent bench stability and ease of removal under mild acidic conditions. This compound functions reliably in multi-step synthetic sequences requiring orthogonal protection and functionalization.
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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: