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Structure of 27006-76-4
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5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxaldehyde features a chlorinated pyrazole core with dual methyl substituents and a reactive aldehyde group. This electron-deficient heterocycle integrates readily into synthetic scaffolds requiring polar, sterically constrained platforms. The aldehyde moiety enables efficient coupling reactions under mild conditions, facilitating rapid assembly of functionalized molecular architectures in medicinal chemistry and materials synthesis.
5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyrazole scaffolds via coupling and functionalization reactions. The aldehyde group facilitates nucleophilic additions and condensation processes, while the chloro and methyl substituents provide orthogonal reactivity for further derivatization. Its bench-stable nature and compatibility with standard reaction conditions make 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: