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Structure of 72187-91-8
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2-Aminopropanenitrile hydrochloride offers a stable, moisture-tolerant source of the α-amino nitrile functionality. This bench-stable salt integrates readily into synthetic sequences requiring nucleophilic amine equivalents or cyanide donors. The protonated amine enhances solubility in polar solvents, streamlining handling in aqueous or mixed-phase reactions.
2-Aminopropanenitrile hydrochloride serves as a versatile building block in synthetic organic chemistry, enabling efficient access to β-amino nitriles and related heterocyclic scaffolds. Its bench-stable form facilitates handling and purification, while the nitrile and amine functionalities support diverse transformations including cyclizations, nucleophilic additions, and metal-catalyzed couplings. Widely employed in medicinal chemistry and process development, it functions as a key intermediate for bioactive molecule synthesis.
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Lot numbers can be found on the outside label of a product: