Diisopinocampheylborane

• CAT Number: R016570
• CAS Number: 21947-87-5
• Molecular Formula: C₂₀H₃₅B
• Molecular Weight: 286.3
• Purity: ≥95%
• Synonyms: d-Diisopinocampheylborane; (+)-Diisopinocampheylborane; Bis(d-isopinocampheyl)borane; [1S-[1α,2β,3α(1R*,2S*,3R*,5R*),5α]]-Bis(2,6,6-trimethylbicyclo[3.1.1]hept-3-yl)borane; Bis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]borane
• Storage: Room temperature
• InChI: 1S/C20H34B/c1-11-15-7-13(19(15,3)4)9-17(11)21-18-10-14-8-16(12(18)2)20(14,5)6/h11-18H,7-10H2,1-6H3
• InChIKey: MPQAQJSAYDDROO-UHFFFAOYSA-N
• SMILES: [B](C1CC2CC(C1C)C2(C)C)C3CC4CC(C3C)C4(C)C

Diisopinocampheylborane is an organoboron compound known for its utility in asymmetric synthesis. This reagent features two isopinocampheyl groups, which confer high selectivity and efficiency in catalytic reactions, particularly in the hydroboration of alkenes and alkynes. Its chiral nature allows for the introduction of chirality into organic molecules, making it valuable in the synthesis of enantiomerically enriched compounds. Research into diisopinocampheylborane focuses on its applications in pharmaceuticals and fine chemicals, as well as its role in developing new synthetic methodologies.