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Structure of 16932-49-3
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2,6-Dimethoxybenzonitrile features a nitrile group flanked by two methoxy substituents at the 2 and 6 positions of the benzene ring. This electron-donating substitution pattern enhances solubility in polar organic solvents while maintaining stability under standard bench conditions. The molecule serves as a valuable building block in synthetic organic chemistry, particularly for constructing functionalized aromatic scaffolds via cross-coupling or electrophilic substitution reactions.
2,6-Dimethoxybenzonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized aromatic scaffolds. Its ortho-dimethoxy substitution pattern enhances solubility and stability while the nitrile group provides a reliable handle for reductive transformations, amidation, or cyclization reactions. This compound facilitates streamlined synthesis of heterocyclic intermediates and is well-suited for bench-scale applications requiring robust handling and predictable reactivity.
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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: