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Atomfair (2s,3s)-1,4-Dibromobutane-2,3-diol C4H8Br2O2

Description (2S,3S)-1,4-Dibromobutane-2,3-diol (CAS No. 14396-65-7) is a high-purity chiral diol derivative with the molecular formula C4H8Br2O2. This compound features two bromine atoms and two hydroxyl groups in a stereospecific (2S,3S) configuration, making it a valuable intermediate in asymmetric synthesis and pharmaceutical research. Its rigid structure and reactive functional groups enable its use in cross-coupling reactions, nucleophilic substitutions, and as a precursor for chiral ligands or catalysts. Available in >98% purity (HPLC/GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in sensitive applications. Packaged under inert gas to prevent degradation, it is ideal for researchers requiring precise…

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Description

Description

(2S,3S)-1,4-Dibromobutane-2,3-diol (CAS No. 14396-65-7) is a high-purity chiral diol derivative with the molecular formula C4H8Br2O2. This compound features two bromine atoms and two hydroxyl groups in a stereospecific (2S,3S) configuration, making it a valuable intermediate in asymmetric synthesis and pharmaceutical research. Its rigid structure and reactive functional groups enable its use in cross-coupling reactions, nucleophilic substitutions, and as a precursor for chiral ligands or catalysts. Available in >98% purity (HPLC/GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in sensitive applications. Packaged under inert gas to prevent degradation, it is ideal for researchers requiring precise stereochemical control.

  • CAS No: 14396-65-7
  • Molecular Formula: C4H8Br2O2
  • Molecular Weight: 247.91
  • Exact Mass: 247.88706
  • Monoisotopic Mass: 245.88910
  • IUPAC Name: (2S,3S)-1,4-dibromobutane-2,3-diol
  • SMILES: C([C@H]([C@@H](CBr)O)O)Br
  • Synonyms: (2s,3s)-1,4-dibromobutane-2,3-diol, 299-70-7, (+/-)-1,4-DIBROMO-2,3-BUTANEDIOL, (+,-)-1,4-Dibromo-2,3-dihydroxybutane, 2,3-Butanediol, 1,4-dibromo-, (theta,theta)-(+/-)-

Application

(2S,3S)-1,4-Dibromobutane-2,3-diol serves as a key chiral building block in the synthesis of bioactive molecules, particularly in pharmaceuticals and agrochemicals. Its dibromo functionality allows for further functionalization via Suzuki or Grignard reactions, while the diol group enables chelation or protection strategies. Researchers utilize this compound to develop enantioselective catalysts and investigate stereospecific reaction mechanisms. It is also employed in polymer science for modifying resin properties.

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