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Structure of 94994-15-7
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Methyl 4-(hydroxymethyl)bicyclo[2.2.2]octane-1-carboxylate features a rigid bicyclic framework that imparts exceptional conformational stability, enabling precise spatial control in synthetic transformations. The pendant hydroxymethyl group offers a versatile handle for selective derivatization, while the ester functionality supports downstream functional group interconversion under standard conditions. This scaffold combines steric integrity with reactive accessibility, making it valuable in targeted synthesis and molecular design.
Methyl 4-(hydroxymethyl)bicyclo[2.2.2]octane-1-carboxylate serves as a versatile synthetic building block for strained bicyclic frameworks, enabling efficient access to functionalized cyclohexane and cyclooctane derivatives. The hydroxymethyl group facilitates selective oxidation, protection, or derivatization, while the ester functionality supports subsequent transformations such as reduction or amidation. Its rigid bicyclo[2.2.2]octane core offers enhanced metabolic stability and conformational constraint, making it valuable in medicinal chemistry and target-oriented synthesis.
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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: