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Structure of 703-23-1
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2'-Hydroxy-6'-methoxyacetophenone features a strategically positioned hydroxyl group and methoxy substituent on the aromatic ring, enabling enhanced solubility and stability in polar solvents. This electron-rich scaffold facilitates direct integration into complex molecular architectures without requiring protection steps. The ortho-hydroxy functionality supports chelation in metal-catalyzed transformations, while the para-methoxy group modulates electronic properties for tailored reactivity.
2'-Hydroxy-6'-methoxyacetophenone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted benzofurans and other oxygenated heterocycles via intramolecular cyclization. Its ortho-hydroxyl and para-methoxy functionalities provide complementary reactivity for palladium-catalyzed coupling and electrophilic substitution reactions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science applications.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: