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Structure of 1710-66-3
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(1,2-Thiazol-5-yl)methanol features a reactive thiazole ring fused to a primary alcohol group, enabling direct functionalization in heterocyclic synthesis. This bench-stable, moisture-tolerant scaffold integrates readily into pharmaceutical intermediates and ligand design, offering a versatile handle for C–H activation and cross-coupling transformations under mild conditions.
(1,2-Thiazol-5-yl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to thiazole-containing scaffolds via standard functional group interconversions. Its aldehyde functionality facilitates nucleophilic additions, reductive aminations, and coupling reactions with broad functional group tolerance. The compound exhibits good bench stability and ease of purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process 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: