IUPAC Name: | [2-chloro-5-(trifluoromethyl)phenyl]boronic acid |
Description: | Reactant for: Synthesis of aryl- and hetarylfurocoumarins via Suzuki reaction; Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction; Preparation of xanthines via one-pot coupling with diaminouracil; Pd-catalyzed Suzuki-Miyaura coupling with 8-bromo-1,5-naphthyridin-2-one. May contain varying amounts of anhydride. |
Molecular Weight: | 224.37 |
Molecular Formula: | C7H5ClF3O2B |
Canonical SMILES: | B(C1=C(C=CC(=C1)C(F)(F)F)Cl)(O)O |
InChI: | InChI=1S/C7H5BClF3O2/c9-6-2-1-4(7(10,11)12)3-5(6)8(13)14/h1-3,13-14H |
InChI Key: | YVMXEHZEYONARR-UHFFFAOYSA-N |
Boiling Point: | 303.2 °C at 760 mmHg |
Density: | 1.49 g/cm3 |
MDL: | MFCD00797335 |
LogP: | 1.03860 |
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
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