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Structure of 2089041-34-7
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4-Bromo-1-methyl-1H-indazole-6-carbonitrile features a sterically accessible indazole core with complementary electron-deficient functionality. The bromo and nitrile groups enable direct coupling in cross-coupling reactions, while the methyl substitution enhances solubility and stability under standard conditions. This compound serves as a key building block for bioactive heterocycles in medicinal chemistry.
4-Bromo-1-methyl-1H-indazole-6-carbonitrile serves as a versatile building block for medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its bromo and nitrile functionalities. The methyl group enhances metabolic stability, while the indazole core provides a rigid, bioisosteric scaffold. Bench-stable and compatible with standard purification methods, it facilitates efficient synthesis of complex heterocyclic architectures.
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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 : H315-H319-H320
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P362
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Lot numbers can be found on the outside label of a product: