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Structure of 2941-58-4
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2-Bromo-6-methoxybenzothiazole features a benzothiazole core functionalized with bromine and methoxy groups at the 2- and 6-positions, respectively. This configuration enables direct electrophilic substitution and facilitates cross-coupling reactions in synthetic workflows. The molecule exhibits enhanced solubility in organic media and stability under standard bench conditions. It serves as a key scaffold for constructing bioactive heterocycles and advanced materials.
2-Bromo-6-methoxybenzothiazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromine substituent and electron-rich methoxy group. The benzothiazole core provides robust scaffold functionality for constructing bioactive heterocycles, with excellent bench stability and compatibility in standard coupling protocols.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: