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*For research and further manufacturing use only, not for direct human use.
Structure of 23780-13-4
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This bench-stable, moisture-tolerant building block features a phenylthiazole core with a reactive alcohol handle. The para-positioned phenyl group enhances electron delocalization, while the aldehyde functionality enables direct coupling or oxidation to carboxylic acid derivatives in synthetic workflows.
(2-Phenylthiazol-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based scaffolds. Its benzyl-like functionality facilitates electrophilic coupling and oxidation to carboxylic acid derivatives. The molecule exhibits bench stability, tolerates common functional groups, and functions effectively in standard cross-coupling and derivatization protocols.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: