673854
4-Nitrophenylboronsäure
≥95.0%
Synonym(e):
4-Nitrobenzeneboronic acid, p-Nitrophenylboronic acid, p-nitro-benzeneboronic acid
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Alle Fotos(3)
About This Item
Lineare Formel:
(O2N)C6H4(B(OH)2)
CAS-Nummer:
Molekulargewicht:
166.93
MDL-Nummer:
UNSPSC-Code:
12352103
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
Assay
≥95.0%
Form
solid
mp (Schmelzpunkt)
285-290 °C (dec.)
Funktionelle Gruppe
nitro
SMILES String
OB(O)c1ccc(cc1)[N+]([O-])=O
InChI
1S/C6H6BNO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4,9-10H
InChIKey
NSFJAFZHYOAMHL-UHFFFAOYSA-N
Anwendung
Reagent used for
Reagent used in Preparation of
- 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
Sonstige Hinweise
May contain varying amounts of anhydride
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