673854
4-Nitrophenylboronic acid
≥95.0%
Synonym(s):
4-Nitrobenzeneboronic acid, p-Nitrophenylboronic acid, p-nitro-benzeneboronic acid
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Linear Formula:
(O2N)C6H4(B(OH)2)
CAS Number:
Molecular Weight:
166.93
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
≥95.0%
form
solid
mp
285-290 °C (dec.)
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
InChI key
NSFJAFZHYOAMHL-UHFFFAOYSA-N
Application
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
Other Notes
May contain varying amounts of anhydride
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Ying Liu et al.
Chemosphere, 247, 125837-125837 (2020-01-14)
Application of low dosage of H2O2 at early stage of cyanobacterial life cycle is a promising route for cyanobacterial bloom mitigation, which could minimize adverse effects on non-target organisms. Besides, influence of co-existing contaminants on cyanobacterial bloom mitigation under combined
David A Degoey et al.
Journal of medicinal chemistry, 54(20), 7094-7104 (2011-09-09)
Because there is currently no cure for HIV infection, patients must remain on long-term drug therapy, leading to concerns over potential drug side effects and the emergence of drug resistance. For this reason, new and safe antiretroviral agents with improved
Tetrahedron, 63, 6131-6131 (2007)
Rhodium-grafted hydrotalcite catalyst for heterogeneous 1,4-addition reaction of organoboron reagents to electron deficient olefins
Motokura, K.; et al.
Green Chemistry, 13, 2416-2422 (2011)
Copper-catalyzed arylation of indolin-2,3-ones with arylboronic acids
J. Zhang, et al.,
Tetrahedron, 67, 9347-9351 (2011)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service