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CAS 67826-92-0

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(-)-isopinocampheylborane tmeda complex

Description:
(-)-Isopinocampheylborane TMEDA complex is a chiral organoboron compound known for its utility in asymmetric synthesis, particularly in the field of organic chemistry. This compound features a boron atom coordinated to a chiral isopinocampheyl group, which imparts stereochemical control in reactions. The presence of TMEDA (N,N,N',N'-tetramethylethylenediamine) enhances the solubility and reactivity of the borane complex, making it a valuable reagent in various transformations, including hydroboration and alkylation reactions. The compound is typically characterized by its ability to selectively form bonds with specific substrates, leading to the production of enantiomerically enriched products. Its chiral nature allows for the introduction of asymmetry in synthetic pathways, which is crucial in the development of pharmaceuticals and fine chemicals. Additionally, (-)-isopinocampheylborane TMEDA complex is often handled under inert atmospheres due to its sensitivity to moisture and air, which can affect its reactivity and stability. Overall, this compound is a significant tool in modern synthetic organic chemistry.
Formula:C26H54B2N2
InChI:InChI=1/2C10H19B.C6H16N2/c2*1-6-8-4-7(5-9(6)11)10(8,2)3;1-7(2)5-6-8(3)4/h2*6-9H,4-5,11H2,1-3H3;5-6H2,1-4H3/t2*6-,7-,8+,9-;/m11./s1
Synonyms:
  • R-alpine-boramine
  • N,N,N',N'-tetramethylethane-1,2-diamine - [(1S,2S,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]borane (1:2)
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