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Structure of 89187-40-6
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1,3-Dimethyl-1H-pyrazole-5-carbohydrazide features a pyrazole core with methyl and carbohydrazide substituents, enabling direct integration into heterocyclic scaffolds. The hydrazide group facilitates coupling reactions under mild conditions, while the electron-rich pyrazole ring enhances stability and reactivity in synthetic transformations. This compound serves as a key intermediate for bioactive molecule synthesis.
1,3-Dimethyl-1H-pyrazole-5-carbohydrazide serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyrazole-based scaffolds through condensation and cyclization reactions. Its hydrazide functionality facilitates coupling with carbonyl compounds, while the methylated pyrazole core provides enhanced stability and solubility. Ideal for medicinal chemistry campaigns and API intermediate development, it offers predictable reactivity and straightforward purification, making it well-suited for high-throughput and scale-up 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: