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| | 1,3,2-Dioxaborolane, 2-(dichloroMethyl)-4,4,5,5-tetraMethyl- Basic information |
| Product Name: | 1,3,2-Dioxaborolane, 2-(dichloroMethyl)-4,4,5,5-tetraMethyl- | | Synonyms: | 1,3,2-Dioxaborolane, 2-(dichloroMethyl)-4,4,5,5-tetraMethyl-;Dichloromethyl pinacolboronate;Pinacol (dichloromethyl) boronate >=95%;2-(Dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane（WS203860）;(Dichloromethyl)boronic Acid Pinacol Ester;2-(dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;Pinacol (dichloromethyl) boronate | | CAS: | 83622-41-7 | | MF: | C7H13BCl2O2 | | MW: | 210.89 | | EINECS: | | | Product Categories: | | | Mol File: | 83622-41-7.mol |  |
| | 1,3,2-Dioxaborolane, 2-(dichloroMethyl)-4,4,5,5-tetraMethyl- Chemical Properties |
| Boiling point | 103 °C(Press: 20 Torr) | | density | 1.1423 | | refractive index | n/D 1.4511 | | form | liquid |
| | 1,3,2-Dioxaborolane, 2-(dichloroMethyl)-4,4,5,5-tetraMethyl- Usage And Synthesis |
| Uses | Pinacol (dichloromethyl) boronate is a general reagent that was employed by Prof. Greg C. Fu and coworkers to achieve the iterative synthesis of asymmetric (secondary) alkyl boronate esters. These can be further derivatized through a growing suite of chemical transformations developed in the last decade (cross coupling, oxidation, amination, halogenation) that proceed with stereochemical fidelity. |
| | 1,3,2-Dioxaborolane, 2-(dichloroMethyl)-4,4,5,5-tetraMethyl- Preparation Products And Raw materials |
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