IUPAC Name: | (3,5-dibromophenyl)boronic acid |
Description: | Reactant involved in: Vacuo condensation and on-surface radical addition for synthesis of phenylene-boroxine networks; Lithiation of dihalophenyl dioxazaborocines yielding functionalized dihalophenylboronic acids; Cycloboronation of tetrasubstituted butanetetraols; Homocoupling of arylboronic acids; Synthesis of borondipyrromethene hybrids; Studies of structure and activity of NHC and dendritic NHC iridium complexes. |
Molecular Weight: | 279.72 |
Molecular Formula: | C6H5Br2O2B |
Canonical SMILES: | B(C1=CC(=CC(=C1)Br)Br)(O)O |
InChI: | InChI=1S/C6H5BBr2O2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,10-11H |
InChI Key: | WQBLCGDZYFKINX-UHFFFAOYSA-N |
Boiling Point: | 382.8 °C at 760 mmHg |
Melting Point: | >300 °C (lit.) |
Flash Point: | Not applicable |
Purity: | ≥ 95 % |
Density: | 2.09 g/cm3 |
Appearance: | Light pink powder |
Storage: | Keep in dark place, Sealed in dry, Room Temperature |
MDL: | MFCD01075725 |
LogP: | 0.89140 |
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
4-(3,5-Dimethyl-1-pyrazolyl)phenylboronic Acid Pinacol Ester
3-[[2-(Trimethylsilyl)ethoxy]methyl]-3H-imidazo[4,5-b]pyridine-6-boronic Acid Pinacol Ester
Customers Also Viewed
Copyright © 2024 BOC Sciences. All rights reserved.
Our Products