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Structure of 478148-60-6
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Furo[2,3-c]pyridin-5-ylmethanol features a fused heterocyclic core combining furan and pyridine rings, delivering enhanced electronic properties. The pendant hydroxymethyl group enables direct functionalization, facilitating incorporation into bioactive scaffolds. This bench-stable, moisture-tolerant building block supports efficient derivatization under standard conditions.
Furo[2,3-c]pyridin-5-ylmethanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to fused polycyclic scaffolds. Its benzylic alcohol functionality facilitates straightforward oxidation to the carboxylic acid or conversion to esters and other derivatives. The molecule exhibits good bench stability and functional group tolerance, supporting diverse transformations 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-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: