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Structure of 636-72-6
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2-Thiophenemethanol features a thiophene ring fused with a reactive benzylic alcohol, enabling straightforward derivatization. This bench-stable compound integrates readily into synthetic sequences requiring heterocyclic scaffolds with pendant functional handles. The hydroxymethyl group facilitates coupling reactions under standard conditions.
2-Thiophenemethanol serves as a versatile building block in synthetic organic chemistry, enabling efficient functionalization at the benzylic position. Its thiophene ring imparts stability and favorable electronic properties, while the primary alcohol facilitates derivatization via oxidation, esterification, or coupling reactions. The compound exhibits good bench stability and is readily purified by distillation or chromatography, making it suitable for use in medicinal chemistry, catalyst design, and the synthesis of heterocyclic scaffolds.
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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 : H227-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: