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Structure of 35134-07-7
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3-Methoxy-2-thiophenecarboxaldehyde features a thiophene ring fused with an electron-rich methoxy group and a reactive aldehyde handle. This combination enables direct incorporation into heterocyclic scaffolds, offering enhanced solubility and stability under standard bench conditions for synthetic applications in medicinal chemistry and materials science.
3-Methoxy-2-thiophenecarboxaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted thiophene derivatives via standard coupling and functional group transformation protocols. Its aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the methoxy group provides moderate electron donation and enhanced stability under typical reaction conditions. The molecule exhibits favorable bench stability and purification characteristics, making it well-suited for iterative synthetic campaigns 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 : 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: