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Structure of 88888-31-7
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Methyl 4-hydroxybicyclo[2.2.1]heptane-1-carboxylate features a rigid bicyclic framework with a strategically positioned hydroxyl group, enabling precise stereochemical control in synthetic transformations. This bench-stable scaffold integrates readily into complex molecular architectures, offering enhanced regioselectivity in asymmetric synthesis and serving as a key building block for bioactive molecule development.
Methyl 4-hydroxybicyclo[2.2.1]heptane-1-carboxylate serves as a versatile bicyclic building block in synthetic organic chemistry, leveraging the rigid cyclohexane-like framework of the norbornane core. The pendant hydroxyl group enables selective derivatization via esterification, etherification, or oxidation, while the methyl ester supports subsequent hydrolysis or cross-coupling reactions. Its bench-stable nature and compatibility with diverse functional groups make it suitable for medicinal chemistry campaigns requiring conformational constraint and stereochemical control.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: