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Structure of 102522-32-7
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tert-Butyl 8-aminooctanoate features a protected primary amine group flanked by a long aliphatic chain, enabling its use in peptide backbone modification and macrocyclic scaffold synthesis. This bench-stable derivative facilitates efficient coupling reactions under standard conditions, offering enhanced solubility in organic solvents compared to the parent amine.
tert-Butyl 8-aminooctanoate serves as a versatile bifunctional building block in synthetic organic chemistry, enabling straightforward access to amine-containing aliphatic scaffolds. The tert-butyl ester group provides excellent bench stability and facilitates mild acidic deprotection, while the primary amine supports diverse functionalization via acylation, alkylation, or coupling reactions. This compound functions effectively in peptide-like chain extensions and is compatible with standard protecting group strategies, making it valuable for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: