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Structure of 725255-70-9
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tert-Butyl N-(4-methylidenecyclohexyl)carbamate features a stable tert-butyl carbamate protecting group coupled with a cyclohexylidene moiety, enabling efficient incorporation into complex molecular architectures. The electron-rich alkene facilitates downstream functionalization via transition-metal catalysis or cycloaddition reactions. This compound exhibits excellent bench stability and solubility in common organic solvents, streamlining synthetic workflows in medicinal chemistry and natural product synthesis.
tert-Butyl N-(4-methylidenecyclohexyl)carbamate serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized cyclohexane scaffolds. The protected amine and exocyclic alkene functionality offer orthogonal reactivity for downstream transformations, including hydrogenation, electrophilic addition, and transition-metal-catalyzed coupling reactions. Its bench-stable nature and ease of purification make it well-suited for iterative synthesis workflows in medicinal chemistry and process 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: