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Structure of 1246553-15-0
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This tetrahydroindazole derivative features a bromine substituent at the 3-position, enabling direct functionalization in cross-coupling reactions. The saturated indazole core provides enhanced metabolic stability and improved solubility compared to aromatic analogs, making it valuable for medicinal chemistry and drug discovery applications.
3-Bromo-4,5,6,7-tetrahydro-1H-indazole serves as a versatile building block for medicinal chemistry and heterocyclic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and arylalkyl scaffolds. Its saturated indazole core provides enhanced metabolic stability and favorable physicochemical properties, making it well-suited for drug discovery applications. The compound exhibits good bench stability and is readily purified by standard chromatographic methods.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: