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Structure of 1443531-60-9
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This boronate moiety features a methoxy-substituted benzo[b]thiophene scaffold, offering enhanced solubility and stability under standard conditions. The para-methoxy and ortho-methyl groups tune electronic properties for efficient cross-coupling reactions. Ideal for constructing complex heterocyclic architectures in medicinal chemistry and materials science applications.
(7-Methoxy-5-methylbenzo[b]thiophen-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The boronic acid moiety exhibits excellent bench stability and tolerates a range of functional groups, facilitating direct incorporation into complex molecular frameworks. Its utility is particularly notable in the synthesis of heterocyclic scaffolds relevant to medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 3230
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Class : 4.1
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Packing Group : -
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Hazard Statements : H242
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Precautionary Statements : P210-P220-P234-P280-P370+P378-P420-P501
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Lot numbers can be found on the outside label of a product: