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Structure of 63680-90-0
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3-Chloro-1H-pyrazol-4-amine hydrochloride features a pyrazole core with a chlorine substituent at the 3-position and a primary amine at the 4-position, delivering enhanced reactivity for C–N bond formation. The hydrochloride salt ensures high solubility in aqueous media and improved shelf stability under standard conditions. This compound serves as a key intermediate in medicinal chemistry, enabling rapid access to functionalized heterocycles through coupling reactions.
3-Chloro-1H-pyrazol-4-amine hydrochloride serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyrazole scaffolds via palladium-catalyzed coupling and electrophilic functionalization. The chloro group at the 3-position facilitates C–Cl bond activation in cross-coupling reactions, while the amino functionality supports direct derivatization or incorporation into bioactive molecules. Its crystalline solid form ensures bench stability and ease of handling, with purification achievable through simple recrystallization.
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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: