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CAS 99438-28-5

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(+)-B-methoxydiisopinocampheylborane hydrate

Description:
(+)-B-methoxydiisopinocampheylborane hydrate 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 bonded to two isopinocampheyl groups and a methoxy group, contributing to its unique stereochemical properties. The presence of the hydrate indicates that it contains water molecules, which can influence its solubility and reactivity. Typically, this compound is utilized as a reagent in various reactions, including hydroboration and in the synthesis of alcohols from alkenes, showcasing its role in facilitating the formation of carbon-carbon bonds. Its chirality allows for the selective formation of enantiomers, making it valuable in the production of pharmaceuticals and fine chemicals. The compound is generally handled with care due to the reactivity of boron species and should be stored under appropriate conditions to maintain its stability and efficacy.
Formula:C21H37BO
InChI:InChI=1/C21H37BO/c1-12-16-8-14(20(16,3)4)10-18(12)22(23-7)19-11-15-9-17(13(19)2)21(15,5)6/h12-19H,8-11H2,1-7H3/t12-,13-,14-,15-,16+,17+,18+,19+/m1/s1
Synonyms:
  • methyl bis[(1S,2S,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]borinate
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