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Structure of 4146-24-1
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6-Chloro-2-methylbenzo[d]thiazole features a fused benzothiazole core with strategic chlorine and methyl substitutions that enhance electronic modulation and steric profile. This scaffold serves as a robust building block in medicinal chemistry, particularly for kinase inhibitors and fluorescent probes. The electron-deficient ring system facilitates efficient coupling reactions under standard conditions.
6-Chloro-2-methylbenzo[d]thiazole serves as a versatile building block in medicinal chemistry, enabling efficient construction of biologically active heterocycles. Its chloro and methyl groups provide orthogonal reactivity for palladium-catalyzed cross-coupling and electrophilic substitution. The benzo[d]thiazole core exhibits excellent bench stability and facilitates purification via standard chromatographic methods, making it well-suited for scalable synthesis and high-throughput screening campaigns.
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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: