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Structure of 37102-48-0
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2-Methyl-1H-pyrrole-3-carboxylic acid features a sterically hindered pyrrole core with a carboxylic acid group at the 3-position, enabling direct incorporation into peptide and heterocyclic scaffolds. The methyl substitution enhances electronic delocalization and improves solubility in polar organic solvents. This derivative serves as a key building block for bioactive molecule synthesis, particularly in medicinal chemistry and materials science applications.
2-Methyl-1H-pyrrole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrrole-based heterocycles. Its carboxylic acid functionality facilitates direct amidation, esterification, and coupling reactions, while the methyl group enhances metabolic stability. The molecule exhibits bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns and API intermediate 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 : 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: