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Structure of 197364-68-4
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This bench-stable fluorinated benzothiazole derivative features a reactive methanol handle for facile conjugation. The electron-deficient heterocycle enhances compatibility with nucleophilic transformations, while the fluorine substituent improves metabolic stability and membrane permeability in bioactive molecule design.
(6-Fluorobenzo[d]thiazol-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient incorporation of fluorinated benzothiazole motifs into target molecules. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and condensation reactions, while the benzo[d]thiazole core provides metabolic stability and enhanced binding affinity. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis workflows in API development.
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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: