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Structure of 13679-70-4
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5-Methyl-2-thiophenecarboxaldehyde features a conjugated thiophene core with an aldehyde and methyl group positioned for orthogonal reactivity. This bench-stable, moisture-tolerant heterocycle integrates readily into cross-coupling and condensation workflows, enabling efficient access to functionalized thienyl scaffolds in synthetic and medicinal chemistry applications.
5-Methyl-2-thiophenecarboxaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to functionalized thiophene derivatives. Its aldehyde functionality facilitates nucleophilic additions, condensations, and coupling reactions under mild conditions. The methyl group provides steric and electronic modulation, enhancing stability and selectivity in downstream transformations. This compound functions effectively in medicinal chemistry scaffolds and materials science applications, offering reliable reactivity and ease of purification.
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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: