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Structure of 124899-25-8
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cis-1-Methylcyclohexane-1,4-diol features a rigid, chair-conformational scaffold with two hydroxyl groups in cis orientation and a methyl substituent at C1. This configuration enables predictable stereochemical outcomes in asymmetric synthesis, particularly in diol-directed transformations. The compound exhibits enhanced solubility in polar solvents and stability under standard bench conditions, facilitating its use in synthetic intermediates for natural product and pharmaceutical applications.
cis-1-Methylcyclohexane-1,4-diol serves as a valuable chiral building block in synthetic organic chemistry, offering well-defined stereochemistry for asymmetric synthesis. Its equatorial methyl and hydroxyl groups provide enhanced stability and favorable solubility, enabling efficient functionalization in standard transformations. The molecule functions effectively in oxidation, protection, and coupling reactions, facilitating access to complex cyclic architectures relevant to natural product and pharmaceutical intermediates.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: