Other grades of this product :
| 3-Methoxycarbonylphenylboronic acid Basic information |
| 3-Methoxycarbonylphenylboronic acid Chemical Properties |
| Melting point | 205-208 °C(lit.) | | Boiling point | 359.9±44.0 °C(Predicted) | | density | 1.25±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | pka | 7.74±0.10(Predicted) | | form | Powder | | color | White to off-white | | Water Solubility | Reacts with water. | | InChIKey | ALTLCJHSJMGSLT-UHFFFAOYSA-N | | CAS DataBase Reference | 99769-19-4(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 37/39-26-36 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29319090 |
| 3-Methoxycarbonylphenylboronic acid Usage And Synthesis |
| Chemical Properties | White to light yellow crystal powde | | Uses | 3-Methoxycarbonylphenylboronic acid can be used in the preparation of substituted pyrazolylpyrimidinamine derivative for use as protein kinase inhibitors and suzuki reaction.
| | Uses | suzuki reaction | | Uses | 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 acid6, chromenones and their bradykinin B1 antagonistic active, Pt nanoparticles at Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injecti, salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor. |
| 3-Methoxycarbonylphenylboronic acid Preparation Products And Raw materials |
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