IUPAC Name: | [4-[tert-butyl(dimethyl)silyl]oxyphenyl]boronic acid |
Description: | Reactant involved in: Asymmetric addition reactions with β-substituted cyclic enones; Hydroarylation and heterocyclization with phenylpropiolates; Double Suzuki-Miyaura coupling reactionsStarting material for the synthesis of red electroluminescent polyfluorenes. Reactant involved in the synthesis of biologically active molecules including: Phenylpyridone derivatives as MCH1R antagonists; Atromentin and its O-alkylated derivatives; Gelatinases and MT1-MMP inhibitors. |
Molecular Weight: | 252.19 |
Molecular Formula: | C12H21O3BSi |
Canonical SMILES: | B(C1=CC=C(C=C1)O[Si](C)(C)C(C)(C)C)(O)O |
InChI: | InChI=1S/C12H21BO3Si/c1-12(2,3)17(4,5)16-11-8-6-10(7-9-11)13(14)15/h6-9,14-15H,1-5H3 |
InChI Key: | NVHHEADQQACSCJ-UHFFFAOYSA-N |
Boiling Point: | 321.4 °C at 760 mmHg |
Melting Point: | 194-198 °C (lit.) |
Flash Point: | Not applicable |
Purity: | ≥ 95 % |
Density: | 1.01 g/cm3 |
MDL: | MFCD03093888 |
LogP: | 1.75040 |
Customer Support
If the product you need is not in our catalog, please contact us in time to submit your needs. You can help our website get better and better. Why not submit the request today?
Customer Centered
Related Functional Groups
Boronic Acids and Esters
2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine
Customers Also Viewed
Copyright © 2024 BOC Sciences. All rights reserved.
Our Products