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Structure of 145508-94-7
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tert-Butyl 4-(iodomethyl)piperidine-1-carboxylate delivers a reactive iodoalkyl handle for efficient conjugation in synthetic chemistry. This bench-stable, moisture-tolerant reagent features a piperidine core with a pendant iodomethyl group, enabling straightforward alkylation and C–C bond formation under mild conditions. The tert-butyl carbamate protects the amine during transformations while allowing selective deprotection when required.
tert-Butyl 4-(iodomethyl)piperidine-1-carboxylate serves as a versatile synthetic building block for the introduction of piperidine-derived alkylating units. The iodomethyl group enables efficient SN2 reactions with nucleophiles, facilitating C–C and C–heteroatom bond formation under mild conditions. Its tert-butyl carbamate protection offers excellent bench stability and compatibility with diverse reaction environments, simplifying purification and enabling straightforward deprotection to yield the free piperidine amine.
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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: