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Atomfair CID 2773595 Bis(pinanediolato)diboron C20H32B2O4

Description CID 2773595 , also known as Bis[(-)pinanediolato]diboron, is a highly specialized organoboron compound with the molecular formula C20H32B2O4. This chiral boron reagent is widely utilized in asymmetric synthesis and cross-coupling reactions due to its unique structural properties. The IUPAC name, (1R,2S,6R,8R)-2,9,9-trimethyl-4-[(1R,2S,6R,8R)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decane, reflects its intricate bicyclic framework, which enhances stereoselectivity in organic transformations. With a CAS number of 230299-17-9 , this compound is supplied as a high-purity solid, ensuring optimal performance in sensitive applications. Researchers value its role in Suzuki-Miyaura couplings, borylation reactions, and other catalytic processes requiring enantiomeric control.

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Description

Description

CID 2773595, also known as Bis[(-)pinanediolato]diboron, is a highly specialized organoboron compound with the molecular formula C20H32B2O4. This chiral boron reagent is widely utilized in asymmetric synthesis and cross-coupling reactions due to its unique structural properties. The IUPAC name, (1R,2S,6R,8R)-2,9,9-trimethyl-4-[(1R,2S,6R,8R)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decane, reflects its intricate bicyclic framework, which enhances stereoselectivity in organic transformations. With a CAS number of 230299-17-9, this compound is supplied as a high-purity solid, ensuring optimal performance in sensitive applications. Researchers value its role in Suzuki-Miyaura couplings, borylation reactions, and other catalytic processes requiring enantiomeric control.

  • CAS No: 230299-17-9
  • Molecular Formula: C20H32B2O4
  • Molecular Weight: 358.1
  • Exact Mass: 358.2486698
  • Monoisotopic Mass: 358.2486698
  • IUPAC Name: (1R,2S,6R,8R)-2,9,9-trimethyl-4-[(1R,2S,6R,8R)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decane
  • SMILES: B1(O[C@@H]2C[C@H]3C[C@@H]([C@@]2(O1)C)C3(C)C)B4O[C@@H]5C[C@H]6C[C@@H]([C@@]5(O4)C)C6(C)C
  • Synonyms: 230299-17-9, bis[(-)pinanediolato]diboron, (1R,2S,6R,8R)-2,9,9-Trimethyl-4-[(1R,2S,6R,8R)-2,9,9-trimethyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decan-4-yl]-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decane, (-)-Bis(pinanediolato)diboron, AKOS025293621

Application

CID 2773595 is a key reagent in asymmetric borylation reactions, enabling the synthesis of chiral boronic esters with high enantioselectivity. It is particularly valuable in pharmaceutical research for constructing complex molecular architectures. The compound also finds use in materials science for developing boron-containing polymers and catalysts. Its stability and reactivity make it a preferred choice for cross-coupling methodologies.

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