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Structure of 6290-03-5
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(R)-(-)-1,3-Butanediol is a chiral diol featuring a defined stereochemistry at the C1 and C3 positions. This configuration imparts distinct conformational preferences in synthetic transformations. The molecule exhibits enhanced solubility in polar solvents and maintains stability under standard bench conditions. It serves as a valuable building block in asymmetric synthesis, particularly for constructing complex stereodefined intermediates in natural product and pharmaceutical development.
(R)-(-)-1,3-Butanediol serves as a chiral building block for asymmetric synthesis, enabling stereoselective transformations in pharmaceutical and agrochemical development. Its bench-stable, optically pure form facilitates reliable use in nucleophilic substitutions, esterifications, and coupling reactions. The 1,3-diol functionality supports orthogonal protection strategies and functions as a key scaffold in the construction of bioactive heterocycles and complex natural product intermediates.
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Lot numbers can be found on the outside label of a product: