Chemical Properties:
Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, 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: 3-(Methoxycarbonyl)phenylboronic Acid CAS: 99769-19-4Item | Specifications |
Appearance | White to Light Yellow Powder |
Purity / Analysis Method | >97.0% (HPLC) |
Purity | >97.0% (Neutralization Titration) |
Infrared Spectrum | Conforms to Structure |
Proton NMR Spectrum | Conforms to Structure |
Test Standard | Enterprise Standard |
Usage | Pharmaceutical Intermediates |
Description:
Specifications:
Package & Storage:
Chemical Name | 3-(Methoxycarbonyl)phenylboronic Acid |
Synonyms | 3-Methoxycarbonylphenylboronic Acid; 3-(Methoxycarbonyl)benzeneboronic Acid |
CAS Number | 99769-19-4 |
CAT Number | RF-PI1451 |
Stock Status | In Stock, Production Scale Up to Tons |
Molecular Formula | C8H9BO4 |
Molecular Weight | 179.97 |
Melting Point | 205.0~208.0℃ (lit.) |
Solubility | Soluble in Methanol; Insoluble in Water |
Brand | Ruifu Chemical |
Advantages:
FAQ:
Application:
3-(Methoxycarbonyl)phenylboronic Acid (CAS: 99769-19-4), Suzuki-Miyaura Cross Coupling Reaction; Boron Compounds. 3-(Methoxycarbonyl)phenylboronic Acid can be used in the preparation of substituted pyrazolylpyrimidinamine derivative for use as protein kinase inhibitors and suzuki reaction. Reagent used for tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, one-pot ipso-nitration of arylboronic acids, copper-catalyzed nitration, cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling. Reagent used in Preparation of biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid.