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Structure of 203792-32-9
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This aminomethyl-furan nitrile hydrochloride features a reactive nitrile group and a primary amine handle, enabling straightforward functionalization. The protonated amine enhances solubility in aqueous media, while the furan ring provides a stable heteroaromatic scaffold for bioconjugation and medicinal chemistry applications.
5-(Aminomethyl)furan-2-carbonitrile hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to heterocyclic scaffolds via standard functional group transformations. The nitrile group facilitates nucleophilic additions and cyclizations, while the pendant amine supports derivatization through alkylation or acylation. Bench-stable and readily purified, it functions effectively in multi-step syntheses requiring orthogonal reactivity and compatibility with common reaction conditions.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: