4-Nitrophenylboronic Acid

Reagent used for: Ligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings ; Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines ; Diels-Alder or C-H activation reactions ; Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulations; N-arylation of phenylurea using copper acetylacetonate catalyst ; Environmentally benign one-pot synthesis through a double arylation process ; Copper-mediated cyanations ; copper-catalyzed arylations ; Regioselective glycosylations ; Suzuki couplings followed by arylations ; X-ray absorption on rhodium-grafted hydrotalcite catalyst for heterogeneous 1,4-addition reaction of organoboron reagents to electron deficient olefins Reagent used in Preparation of; Combretastatin analogs as potential antitumor agents ; Human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses.

(4-nitrophenyl)boronic acid; (4-nitrophenyl)boronic acid

(4-nitrophenyl)boronic acid

B(C1=CC=C(C=C1)[N+](=O)[O-])(O)O

InChI=1S/C6H6BNO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4,9-10H

NSFJAFZHYOAMHL-UHFFFAOYSA-N

373.7 °C at 760 mmHg

285-290 °C (dec.)

Not applicable

≥ 95.0 %

1.4 g/cm³

-0.20220

H302

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501

Warning