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Structure of 78583-81-0
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5-(4-Chlorophenyl)-1H-pyrazol-3-amine features a pyrazole core functionalized with a chlorophenyl group at C5 and an amino substituent at C3, delivering enhanced electron density and synthetic versatility. This scaffold serves as a key building block in medicinal chemistry, particularly for kinase inhibitors and bioactive heterocycles. The molecule exhibits robust stability under standard conditions and integrates readily into diverse coupling reactions.
5-(4-Chlorophenyl)-1H-pyrazol-3-amine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through palladium-catalyzed cross-coupling and electrophilic substitution reactions. Its robust bench stability, predictable reactivity, and compatibility with diverse functional groups make it ideal for constructing drug-like scaffolds in API development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: