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Structure of 1918-78-1
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2-Methylthiophene-3-carboxylic acid features a conjugated thiophene core with an electron-rich heterocycle and a carboxylic acid group, enabling direct functionalization in cross-coupling reactions. This scaffold offers enhanced solubility in polar organic solvents and stability under standard bench conditions, making it suitable for synthetic intermediates in pharmaceutical and materials chemistry applications.
2-Methylthiophene-3-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its carboxylic acid functionality facilitates direct coupling reactions, while the thiophene core provides robust stability and favorable electronic properties for further functionalization. The methyl group enhances solubility and reactivity in standard transformations, making it well-suited for medicinal chemistry and process development workflows.
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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: