Unsymmetrical Diborane(4) Derivatives: A Comparative Study was written by Borner, Corinna;Wiecha, Maximilian T.;Kleeberg, Christian. And the article was included in European Journal of Inorganic Chemistry in 2017.HPLC of Formula: 1214264-88-6 This article mentions the following:
Since its introduction in 2010 by Suginome et al., pinB-Bdan [pin = OCMe2CMe2O, dan = (NH)2(C10H6)] has become a valuable reagent in various regioselective (bis)borylation reactions, and related unsym. diborane(4) derivatives were used as versatile precursors for diaminoboryl complexes. However, the unsym. diborane(4) derivatives employed show little variation of the diol and diamine moieties. The present study expands this class of compounds and reports the synthesis of unsym. diborane(4) derivatives [C2H4(tBuN)2]B-B(NMe2)2 and [C2H4(tBuN)2]B-B(NMe2)Cl, bearing a sterically demanding nonaromatic diamine moiety, as well as [C6H4(HN)2]B-B(O2C5H10), [C6H4(HN)2]B-B(O2C2H4), and [C6H4(HN)2]B-B[O2C6H2(C2H9)2], which illustrate the variability of the diol moiety. Fully characterization of all compounds including single-crystal x-ray diffraction studies allows for the 1st time a comparative discussion of the spectroscopic and structural properties of this class of compounds In the experiment, the researchers used many compounds, for example, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6HPLC of Formula: 1214264-88-6).
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine (cas: 1214264-88-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.HPLC of Formula: 1214264-88-6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts