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Structure of 1197193-46-6
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3-Amino-7-chloro-5-nitro-1H-indazole features a fused bicyclic core with complementary electron-withdrawing and donating substituents, enabling precise tuning of reactivity in heterocyclic synthesis. The amino group facilitates nucleophilic coupling, while the chloro and nitro functionalities offer orthogonal handles for cross-coupling and reduction strategies under standard conditions. This scaffold delivers structural diversity in medicinal chemistry applications.
3-Amino-7-chloro-5-nitro-1H-indazole serves as a versatile building block in medicinal chemistry, enabling the construction of nitrogen-rich heterocyclic scaffolds. Its complementary functional groups—amino, chloro, and nitro—facilitate sequential transformations including cross-coupling, nucleophilic substitution, and reduction sequences. The molecule exhibits bench stability and compatibility with standard purification protocols, supporting its use in multi-step synthesis of potential API candidates and functional materials.
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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: