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Structure of 18677-48-0
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3,5-Dimethoxypyridine features two methoxy groups positioned at the 3- and 5-positions of the pyridine ring, creating a symmetric, electron-rich heteroaromatic scaffold. This configuration enhances solubility in organic solvents while maintaining bench-stable handling characteristics. The compound serves as a key building block in medicinal chemistry for constructing bioactive molecules, particularly where moderate electron density and controlled polarity are required.
3,5-Dimethoxypyridine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through cross-coupling and electrophilic substitution reactions. Its ortho-dimethoxy substitution pattern enhances solubility and facilitates functionalization at the 2- and 6-positions, while maintaining bench stability and ease of purification. The molecule functions effectively as a synthetic handle in transition-metal-catalyzed transformations, supporting the development of diverse API candidates.
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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: