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Structure of 1638760-94-7
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This boronate moiety integrates seamlessly into Suzuki-Miyaura coupling reactions, offering enhanced reactivity and stability under standard conditions. The electron-rich pyrrolopyridine scaffold enables efficient cross-coupling with aryl halides, while the pendant amine group facilitates downstream functionalization through amide bond formation or conjugation chemistry.
(2-Methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine serves as a versatile building block for medicinal chemistry, enabling efficient access to pyrrolopyridine-based scaffolds. Its primary amine functionality facilitates straightforward derivatization via amidation, alkylation, and reductive amination. The molecule exhibits good bench stability and compatibility with standard purification methods, supporting its use in multi-step synthesis and high-throughput screening campaigns.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314-H318-H335
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: