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Structure of 39068-88-7
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This phenolic compound features a methyl group at the 6-position and methoxy substituents at carbons 2, 3, and 4, creating a sterically shielded, electron-rich aromatic system. The extended methoxy substitution enhances solubility in organic solvents and improves stability under standard bench conditions. This combination enables direct use in synthetic routes requiring hindered, polarizable aryl donors.
2,3,4-Trimethoxy-6-methylphenol serves as a valuable building block in medicinal chemistry and natural product synthesis, offering orthogonal methoxy groups for selective derivatization and a methyl-substituted aromatic core that enhances metabolic stability. Its bench-stable nature and compatibility with standard coupling and functional group transformation protocols enable efficient access to complex phenolic scaffolds used 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: