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Structure of 2644-93-1
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1,3,5-Trimethyl-1H-pyrazole-4-carbaldehyde features a pyrazole core with three methyl groups enhancing solubility and stability. The aldehyde functionality enables direct coupling in multistep syntheses, while the electron-rich aromatic system supports efficient transition-metal-catalyzed transformations. This bench-stable reagent integrates readily into complex molecular architectures requiring precise functional group placement.
1,3,5-Trimethyl-1H-pyrazole-4-carbaldehyde serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. Its pyrazole core provides structural rigidity and metabolic stability, while the aldehyde functionality enables facile derivatization via reductive amination, condensation, or nucleophilic addition reactions. The trimethyl substitution enhances solubility and bench stability, facilitating purification and handling in standard laboratory workflows. This compound functions effectively in the synthesis of heterocyclic scaffolds and functionalized ligands for drug discovery 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: