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Structure of 98873-55-3
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2-(1H-Imidazol-1-yl)acetonitrile features a polar imidazole ring conjugated to a nitrile-bearing acetyl side chain, enabling strong coordination in transition metal complexes and facilitating nucleophilic functionalization. This bench-stable compound integrates readily into ligand design for catalysis and serves as a key scaffold in bioactive molecule synthesis.
2-(1H-Imidazol-1-yl)acetonitrile serves as a versatile building block in synthetic organic chemistry, enabling the construction of imidazole-containing scaffolds through nucleophilic substitution and coupling reactions. The nitrile group provides a handle for further functionalization, while the imidazole moiety offers hydrogen-bonding capacity and potential for metal coordination. Bench-stable and compatible with a range of reaction conditions, it facilitates efficient access to heterocyclic intermediates relevant to medicinal chemistry and agrochemical development.
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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: