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Structure of 23690-49-5
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2-(1H-Indol-5-yl)acetonitrile features a conjugated indole scaffold linked to a nitrile group, enabling integration into bioactive molecule scaffolds. This bench-stable derivative exhibits favorable solubility in organic solvents and serves as a key intermediate for pharmaceutical and agrochemical synthesis.
2-(1H-Indol-5-yl)acetonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through nucleophilic addition and subsequent functionalization. The nitrile group facilitates selective transformations, including hydrolysis to carboxylic acids or reduction to primary amines, while the indole core supports diverse derivatization under standard reaction conditions. Its bench-stable nature and compatibility with common coupling protocols make it a practical choice for synthesis of bioactive molecules and heterocyclic intermediates.
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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: