Chemical Properties:
Package: Bottle, 25kg/Barrel, or according to customer's requirement. Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.Manufacturer Supply With High Quality, Commercial Production Chemical Name: Allylboronic Acid Pinacol Ester CAS: 72824-04-5Item | Specifications |
Appearance | Colorless to Pale Yellow Liquid |
Purity / Analysis Method | >98.0% (GC) |
Stabilized With Phenothiazine | <2.00% |
Total Impurities | <2.00% |
Test Standard | Enterprise Standard |
Usage | Pharmaceutical Intermediates |
Description:
Specifications:
Package & Storage:
Chemical Name | Allylboronic Acid Pinacol Ester (Stabilized With Phenothiazine) |
Synonyms | 2-Allyl-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane; 2-(Prop-2-en-1-yl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane (Stabilized With Phenothiazine) |
CAS Number | 72824-04-5 |
CAT Number | RF-PI1390 |
Stock Status | In Stock, Production Scale Up to Tons |
Molecular Formula | C9H17BO2 |
Molecular Weight | 168.04 |
Boiling Point | 50.0~53.0℃/5 mmHg (lit.) |
Density | 0.896 g/ml at 25℃ (lit.) |
Refractive Index (N20/D) | 1.425~1.427 |
Brand | Ruifu Chemical |
Advantages:
FAQ:
Application:
Allylboronic Acid Pinacol Ester (CAS: 72824-04-5) can act as reagent used for Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions and olefin metathesis; Intermolecular radical additions; Allylboration of aldehydes catalyzed by chiral spirobiindane diol (SPINOL) based phosphoric acids and Cobalt-catalyzed regioselective hydrovinylation of dienes with alkenes; Nucleic acid-templated energy transfer leading to a photorelease reaction and stereoselective indium-catalyzed Hosomi-Sakurai reactions. Allylboronic Acid Pinacol Ester reacts with carboxylic acids, in the presence of tri-n-butyltin hydride, to give homoallylic alcohols in good yield. Homoallylic alcohols can also be formed by allylboration of aldehydes.