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Structure of 931-17-9
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1,2-Cyclohexanediol offers a rigid, vicinal diol architecture ideal for stereocontrolled transformations. This bench-stable compound features high solubility in polar solvents and serves as a reliable chiral synthon in asymmetric synthesis. The adjacent hydroxyl groups enable efficient derivatization through oxidation, protection, or cyclization reactions.
1,2-Cyclohexanediol serves as a versatile diol building block in synthetic organic chemistry, enabling stereoselective transformations through its well-defined cis-configuration. Its bench-stable nature and compatibility with common protecting group strategies facilitate efficient functionalization in complex molecule synthesis. The compound functions effectively in oxidation, acetal formation, and coupling reactions, supporting applications in natural product synthesis and pharmaceutical intermediate development.
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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: