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Structure of 4925-88-6
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2,5-Dimethoxy-4-methylbenzaldehyde features a benzaldehyde core with ortho-methoxy and para-methyl substituents, delivering enhanced electron density and steric bulk. This configuration promotes stability and reactivity in electrophilic aromatic substitution and transition-metal-catalyzed coupling processes. The aldehyde functionality enables direct incorporation into complex molecular architectures via condensation or oxidation reactions.
2,5-Dimethoxy-4-methylbenzaldehyde serves as a versatile building block in the synthesis of bioactive heterocycles and aromatic scaffolds. Its aldehyde functionality enables efficient imine formation and reductive amination, while the ortho-dimethoxy and methyl substituents provide enhanced stability and favorable electronic effects for electrophilic substitution. The compound exhibits excellent bench stability and is compatible with standard purification techniques, facilitating its use in medicinal chemistry campaigns and multi-step syntheses.
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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: