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Structure of 103262-35-7
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This bench-stable benzofuran scaffold integrates a reactive primary alcohol at the 5-position, enabling straightforward functionalization. The fused ring system imparts rigidity and enhanced metabolic stability, making it valuable for medicinal chemistry campaigns targeting CNS-penetrant therapeutics.
(2,3-Dihydrobenzofuran-5-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocycles. Its benzylic alcohol functionality facilitates straightforward derivatization via oxidation, protection, or coupling reactions. The dihydrobenzofuran core imparts metabolic stability and favorable pharmacokinetic properties, making it valuable for scaffold elaboration in API development. Bench-stable and compatible with standard synthetic protocols, it functions effectively in multi-step synthesis 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: