Atomfair tert-butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl)acetate C13H22O5

Description tert-butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl)acetate (CAS No. 124752-23-4) is a high-purity chiral intermediate with the molecular formula C13H22O5. This compound features a dioxane ring with formyl and tert-butyl acetate functional groups, making it a valuable building block for asymmetric synthesis and pharmaceutical research. Its stereochemistry ( 4R,6S ) ensures precise reactivity in enantioselective transformations. Ideal for use in API development, catalysis, and fine chemical synthesis, this product is rigorously tested for identity, purity, and stability via HPLC, GC, and NMR. Supplied in sealed containers under inert gas to prevent degradation.

Description

Description

tert-butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl)acetate (CAS No. 124752-23-4) is a high-purity chiral intermediate with the molecular formula C13H22O5. This compound features a dioxane ring with formyl and tert-butyl acetate functional groups, making it a valuable building block for asymmetric synthesis and pharmaceutical research. Its stereochemistry (4R,6S) ensures precise reactivity in enantioselective transformations. Ideal for use in API development, catalysis, and fine chemical synthesis, this product is rigorously tested for identity, purity, and stability via HPLC, GC, and NMR. Supplied in sealed containers under inert gas to prevent degradation.

  • CAS No: 124752-23-4
  • Molecular Formula: C13H22O5
  • Molecular Weight: 258.31
  • Exact Mass: 258.14672380
  • Monoisotopic Mass: 258.14672380
  • IUPAC Name: tert-butyl 2-[(4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl]acetate
  • SMILES: CC1(O[C@H](C[C@H](O1)C=O)CC(=O)OC(C)(C)C)C
  • Synonyms: 124752-23-4, tert-Butyl (4R-cis)-6-formaldehydel-2,2-dimethyl-1,3-dioxane-4-acetate, tert-butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl)acetate, Tert-butyl 2-[(4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl]acetate, 123185-87-5

Application

This compound serves as a key chiral synthon in the synthesis of statin-class pharmaceuticals, particularly for side-chain intermediates. It is utilized in asymmetric hydrogenation and cross-coupling reactions to construct complex stereocenters. Researchers also employ it in medicinal chemistry for probing enzyme inhibition or as a precursor to bioactive molecules.

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