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Structure of 1314910-43-4
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This azetidinylidene acetonitrile hydrochloride features a strained azetidine ring fused to an electron-deficient exocyclic double bond, enabling direct nucleophilic addition without preactivation. The protonated nitrogen enhances electrophilicity at the β-carbon, facilitating rapid cycloadditions and conjugate additions under mild conditions. Bench-stable and moisture-tolerant, it serves as a compact, reactive scaffold for heterocyclic synthesis.
2-(Azetidin-3-ylidene)acetonitrile hydrochloride serves as a versatile synthetic building block for constructing nitrogen-containing heterocycles, particularly in the development of pyrrolidine and azetidine derivatives. Its electrophilic α,β-unsaturated nitrile functionality enables efficient Michael additions and cycloaddition reactions under mild conditions. The hydrochloride salt enhances bench stability and solubility, facilitating straightforward handling and purification in standard organic synthesis 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: