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*For research and further manufacturing use only, not for direct human use.
Structure of 3205-34-3
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This chiral diol features a rigid cyclohexane backbone with adjacent hydroxyl groups, enabling precise stereochemical control in asymmetric synthesis. The 1,2-diol motif facilitates selective protection and oxidation reactions, while the bench-stable nature supports reliable use in complex molecular architectures.
((1S,2S)-Cyclohexane-1,2-diyl)dimethanol serves as a chiral building block for asymmetric synthesis, enabling stereoselective transformations in medicinal chemistry and natural product synthesis. Its rigid trans-diol framework provides defined stereochemistry and enhances diastereoselectivity in functionalization reactions. The molecule exhibits excellent bench stability, facilitates straightforward purification, and demonstrates broad compatibility with protecting group strategies and coupling protocols in complex molecule assembly.
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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: