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Structure of 2199-58-8
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3,5-Dimethyl-1H-pyrrole-2-carbaldehyde features a sterically hindered pyrrole core with electron-rich character, enabling selective coupling in transition-metal-catalyzed transformations. The aldehyde functionality provides a handle for diversification via nucleophilic addition or condensation reactions. This bench-stable reagent integrates efficiently into synthetic routes requiring aromatic heterocycles with tunable electronic properties.
3,5-Dimethyl-1H-pyrrole-2-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrrole scaffolds. Its aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the electron-donating methyl groups enhance stability and modulate reactivity. The compound exhibits excellent bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: