IUPAC Name: | [(E)-oct-1-enyl]boronic acid |
Description: | Reactant for: Chiral palladacycle-catalyzed asymmetric ring-opening reaction; Enantioselective conjugate addition catalyzed by acyltartaric acids; Copper-mediated oxidative cross-coupling reactions; Diastereoselective domino Heck-Suzuki reactions. |
Molecular Weight: | 156.03 |
Molecular Formula: | C8H17O2B |
Canonical SMILES: | B(C=CCCCCCC)(O)O |
InChI: | InChI=1S/C8H17BO2/c1-2-3-4-5-6-7-8-9(10)11/h7-8,10-11H,2-6H2,1H3/b8-7+ |
InChI Key: | RBTAJLKAPFBZDQ-BQYQJAHWSA-N |
Boiling Point: | 263.2 °C at 760 mmHg |
Melting Point: | 100-104 °C (lit.) |
Flash Point: | Not applicable |
Purity: | ≥ 95 % |
Density: | 0.911 g/cm3 |
Solubility: | Insoluble in water. Soluble in organic solvents. |
Appearance: | White solid |
MDL: | MFCD02093734 |
LogP: | 1.52500 |
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-(3-Hydroxyphenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
Customers Also Viewed
Copyright © 2024 BOC Sciences. All rights reserved.
Our Products