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Structure of 150349-36-3
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N-(3-Aminopropyl)-N-methylcarbamic acid tert-butyl ester features a protected amine handle ideal for downstream functionalization. The tert-butyl carbamate group ensures stability during synthesis and storage, while the primary amine enables efficient coupling reactions. This reagent integrates seamlessly into peptide extensions, dendrimer assembly, and bioconjugation workflows under standard conditions.
N-(3-Aminopropyl)-N-methylcarbamic acid tert-butyl ester serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient access to nitrogen-containing scaffolds. The tertiary amine and carbamate functionalities offer orthogonal reactivity, facilitating selective derivatization and protection strategies. Its bench-stable nature and compatibility with common coupling conditions make it well-suited for peptide conjugation, fragment-based drug discovery, and the construction of heterocyclic intermediates.
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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: