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Structure of 74168-69-7
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(5-Chlorothiophen-2-yl)methanol features a thiophene core bearing a chlorinated para-position and a reactive hydroxymethyl group. This combination enables direct functionalization in synthetic sequences, particularly useful for coupling reactions and downstream derivatization in medicinal chemistry and materials science applications.
(5-Chlorothiophen-2-yl)methanol serves as a versatile building block for the synthesis of functionalized thiophene derivatives. Its aldehyde functionality enables direct oxidation, reduction, or coupling reactions, while the chlorine substituent supports palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for applications in medicinal chemistry and materials science.
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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: