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Structure of 50289-12-8
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4-Aminotetrahydro-2H-pyran-4-carbonitrile features a pyran ring with a primary amine and nitrile group at the C4 position, offering dual reactivity for conjugate additions and nucleophilic transformations. This bench-stable scaffold integrates readily into heterocyclic frameworks, enabling efficient access to bioactive derivatives in medicinal chemistry.
4-Aminotetrahydro-2H-pyran-4-carbonitrile serves as a versatile scaffold for medicinal chemistry and synthetic organic applications, combining a stable tetrahydropyran ring with orthogonal functional handles: a primary amine and a nitrile group. The molecule enables straightforward derivatization via nucleophilic addition, amidation, or cyclization reactions, and its bench-stable nature supports reliable handling in multi-step syntheses. Functions effectively in the construction of heterocyclic intermediates and bioactive analogs requiring polar, oxygen-rich frameworks with tunable basicity.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H314-H332-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P330+P331-P302+P352-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: