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Structure of 6033-23-4
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(S)-(+)-2-Heptanol can be used as a starting material to synthesize:(S)-(+)-2-benzoyloxyheptane by treating with benzoyl anhydride and Et3N in the presence of DMAP. (S)-2-(p-toluenesulfonyl)heptane by reacting with p-toluenesulfonyl chloride. (+)-2-Heptyl acetate by treating with acetyl chloride.
(S)-Heptan-2-ol serves as a chiral building block for asymmetric synthesis, offering high enantiomeric purity and stability under standard laboratory conditions. Its secondary alcohol functionality enables reliable derivatization—such as oxidation to ketones or conversion to esters and ethers—while maintaining stereochemical integrity. The molecule functions effectively in catalytic asymmetric reactions and is well-suited for the construction of bioactive scaffolds requiring defined stereochemistry.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: