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| IUPAC Name: | 4,4,5,5-tetramethyl-2-[(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]-1,3,2-dioxaborolane |
| Description: | Bis-boronate has been reported by Morken and coworkers to be a key building block in the synthesis of enantioenriched secondary boronate esters, which undergo facile Suzuki-Miyaura coupling with minimal erosion of enantiopurity.Bis[(pinacolato)boryl]methane may be used in the preparation of trans-vinyl boronate esters, via the Boron-Wittig reaction. |
| Molecular Weight: | 267.97 |
| Molecular Formula: | C13H26O4B2 |
| Canonical SMILES: | B1(OC(C(O1)(C)C)(C)C)CB2OC(C(O2)(C)C)(C)C |
| InChI: | InChI=1S/C13H26B2O4/c1-10(2)11(3,4)17-14(16-10)9-15-18-12(5,6)13(7,8)19-15/h9H2,1-8H3 |
| InChI Key: | MQYZGGWWHUGYDR-UHFFFAOYSA-N |
| Melting Point: | 48 °C |
| Storage: | 2-8 °C |
| LogP: | 2.71000 |
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Boronic Acids and Esters
4-(3,5-Dimethyl-1-pyrazolyl)phenylboronic Acid Pinacol Ester
2-(3-Hydroxyphenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
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