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
Quality Level
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
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
Abdallah Hamze et al.
ChemMedChem, 6(12), 2179-2191 (2011-10-13)
A novel class of isocombretastatin A-4 (isoCA-4) analogues with modifications at the 3'-position of the B-ring by replacement with C-linked substituents was studied. Exploration of the structure-activity relationships of theses analogues led to the identification of several compounds that exhibit
Copper-catalyzed arylation of indolin-2,3-ones with arylboronic acids
J. Zhang, et al.,
Tetrahedron, 67, 9347-9351 (2011)
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)
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