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Structure of 3507-27-5
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2-Chloro-4-methoxy-benzothiazole features a chlorinated benzothiazole core with a methoxy group at the para position, delivering enhanced electron-withdrawing character and improved solubility in organic solvents. This scaffold serves as a key building block for pharmaceutical intermediates and functional materials, offering high stability under standard reaction conditions and compatibility with palladium-catalyzed cross-coupling processes.
2-Chloro-4-methoxy-benzothiazole serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloro substituent. The methoxy group enhances solubility and modulates electronic properties, while the benzothiazole core provides stability and compatibility with diverse functional groups. Its bench-stable nature and predictable reactivity make it ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
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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: