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Structure of 192182-55-1
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized indole derivatives with high efficiency. The methyl substitution enhances solubility and stability, enabling reliable use in synthetic workflows without specialized handling.
(1-Methyl-1H-indol-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and heteroaryl halides. Its stability under ambient conditions, compatibility with diverse functional groups, and ease of purification make it well-suited for the synthesis of biologically relevant indole derivatives and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: