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Structure of 106429-07-6
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This bench-stable boronate-bearing heterocycle integrates readily into cross-coupling workflows, offering a robust scaffold for constructing functionalized biaryls. The para-aminobenzothiazole core provides enhanced electron density and solubility in polar solvents, enabling efficient derivatization under mild conditions.
(2-Aminobenzo[d]thiazol-6-yl)methanol serves as a versatile building block in medicinal chemistry, enabling the synthesis of biologically active heterocycles. Its amino and hydroxymethyl functionalities offer orthogonal handles for derivatization, including amide coupling and ether formation. The molecule exhibits good bench stability and facilitates efficient purification via recrystallization or chromatography, making it suitable for scale-up in API development workflows.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: