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: 4-(Methoxycarbonyl)phenylboronic Acid CAS: 99768-12-4| Item | Specifications |
| Appearance | White to Off-White Crystal Powder |
| Purity / Analysis Method | >99.5% (HPLC) |
| Loss on Drying | <0.50% |
| Single Impurity | <0.50% |
| Total Impurities | <0.50% |
| Heavy Metals (as Pb) | <20ppm |
| Infrared Spectrum | Conforms to Structure |
| Test Standard | Enterprise Standard |
| Usage | Pharmaceutical Intermediates |
Description:
Specifications:
Package & Storage:
| Chemical Name | 4-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride) |
| Synonyms | 4-(Methoxycarbonyl)benzeneboronic Acid |
| CAS Number | 99768-12-4 |
| CAT Number | RF-PI1277 |
| Stock Status | In Stock, Production Scale Up to 25 Tons/Month |
| Molecular Formula | C8H9BO4 |
| Molecular Weight | 179.97 |
| Melting Point | 197.0~200.0℃ (lit.) |
| Solubility | Soluble in Methanol; Insoluble in Water |
| Brand | Ruifu Chemical |
Advantages:
FAQ:
Application:
4-(Methoxycarbonyl)phenylboronic Acid (CAS: 99768-12-4) is mainly used as organic synthesis intermediates, pharmaceutical intermediates. 4-(Methoxycarbonyl)phenylboronic Acid is a 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.
