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Structure of 83101-12-6
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4-(3-Hydroxypropyl)benzonitrile features a hydroxylated aliphatic chain appended to a para-cyanophenyl scaffold, delivering enhanced solubility and polarity compared to simple alkyl analogs. This functional group arrangement enables efficient integration into polar reaction systems while maintaining compatibility with standard synthetic transformations. The molecule's balanced hydrophilicity and aromatic stability make it suitable for use in pharmaceutical intermediates and advanced materials synthesis under routine laboratory conditions.
4-(3-Hydroxypropyl)benzonitrile serves as a versatile building block in medicinal chemistry, enabling straightforward derivatization via the hydroxyl and nitrile functionalities. The terminal hydroxyl group facilitates etherification, esterification, or oxidation to carboxylic acid, while the nitrile supports reductive amination or hydrolysis to amide or acid. Its stability under standard bench conditions and compatibility with common coupling reactions make it well-suited for constructing diverse heterocyclic scaffolds and functionalized aryl intermediates in API development.
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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: