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Structure of 221095-80-3
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Azetidin-3-ylmethanamine dihydrochloride delivers a reactive, bench-stable amine handle ideal for conjugation and scaffold diversification. The constrained azetidine ring imparts enhanced metabolic stability, while the protonated diamine form ensures high solubility in aqueous systems. This compound serves as a key building block in medicinal chemistry for targeted peptide coupling and macrocycle formation.
Azetidin-3-ylmethanamine dihydrochloride serves as a versatile building block for the synthesis of bioactive heterocycles, particularly in medicinal chemistry. The compound functions as a key scaffold for constructing azetidine-containing pharmaceuticals due to its enhanced metabolic stability and favorable physicochemical properties. Its amine functionality enables straightforward derivatization via alkylation, acylation, or coupling reactions, while the dihydrochloride salt form ensures excellent solubility and bench stability for routine handling in synthetic workflows.
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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: