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Structure of 267413-32-1
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3-Amino-1H-indazole-6-carbonitrile features a dual functionalization pattern with an amino group and a nitrile moiety positioned at the 3- and 6-positions of the indazole scaffold, enabling direct integration into bioactive molecule design. This electron-deficient heterocycle offers enhanced solubility and stability under standard bench conditions, facilitating efficient coupling reactions in medicinal chemistry workflows.
3-Amino-1H-indazole-6-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to indazole-based scaffolds through standard functional group transformations. The amino and nitrile groups offer orthogonal reactivity for derivatization via coupling, cyclization, or reduction protocols. Bench-stable and readily purified, it facilitates scalable synthesis of kinase inhibitors and other bioactive heterocycles.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: