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Structure of 13589-71-4
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2-Hydroxy-3-methylbenzonitrile features a strategically positioned hydroxyl group adjacent to a nitrile moiety on a methyl-substituted benzene ring. This arrangement enables direct participation in hydrogen bonding and facilitates electrophilic substitution reactions under mild conditions. The compound exhibits enhanced solubility in polar organic solvents and maintains stability during standard bench handling.
2-Hydroxy-3-methylbenzonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted benzimidazoles and other heterocyclic scaffolds. Its ortho-hydroxyl and nitrile groups exhibit complementary reactivity, facilitating cyclization reactions under mild conditions. The methyl substituent enhances metabolic stability and provides a handle for further functionalization, making it valuable in medicinal chemistry and API intermediate synthesis. Bench-stable and readily purified by recrystallization, it functions reliably in standard coupling and condensation 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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: