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Structure of 110860-60-1
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Methyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate features a pyrazole core functionalized with an amino group at C5 and a methyl ester at C4, enabling direct incorporation into diverse heterocyclic scaffolds. The electron-rich pyrazole ring facilitates transition metal-catalyzed coupling reactions, while the amine moiety offers a handle for derivatization under mild conditions. This bench-stable reagent streamlines access to bioactive pyrazole-based compounds in medicinal chemistry.
Methyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrazole scaffolds. The amino and ester functionalities offer orthogonal reactivity for derivatization via amidation, acylation, or coupling reactions. Its bench-stable nature and compatibility with standard synthetic protocols facilitate straightforward purification and integration into medicinal chemistry campaigns targeting kinase inhibitors and other bioactive molecules.
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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: