4-Methoxycarbonylphenylboronic acid,

Code: 594539-1G D2-231

Application

Reagent used forTandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence Copper-mediated ligandless aerobic fluoroalkylation...


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Your Price
€46.30 1G
€56.95 inc. VAT

Application

Reagent used forTandem-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 ofBiaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid† Chromenones and their bradykinin B1 antagonistic activit† Pt nanoparticles@Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injectio† Salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor†

Other Notes

Contains varying amount of anhydride

Packaging

1, 5 g in glass bottle

assay≥95%
formpowder
InChI keyPQCXFUXRTRESBD-UHFFFAOYSA-N
InChI1S/C8H9BO4/c1-13-8(10)6-2-4-7(5-3-6)9(11)12/h2-5,11-12H,1H3
mp197-200 °C (lit.)
Quality Level100
SMILES stringCOC(=O)c1ccc(cc1)B(O)O
Cas Number99768-12-4
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