Learn More
4-Nitrobenzeneboronic acid, 95%
CAS: 24067-17-2 | C6H6BNO4 | 166.93 g/mol
$128.86 - $400.73
Chemical Identifiers
| CAS | 24067-17-2 |
|---|---|
| Molecular Formula | C6H6BNO4 |
| Molecular Weight (g/mol) | 166.93 |
| MDL Number | MFCD00161360 |
| InChI Key | NSFJAFZHYOAMHL-UHFFFAOYSA-N |
| Synonym | 4-nitrophenyl boronic acid, 4-nitrobenzeneboronic acid, p-nitrophenylboronic acid, 4-nitrophenylboronicacid, p-nitrophenyl boronic acid, 4-nitro phenyl boronic acid, boronic acid, 4-nitrophenyl, boronic acid, b-4-nitrophenyl, 4-borononitrobenzene |
| PubChem CID | 2773552 |
| IUPAC Name | (4-nitrophenyl)boronic acid |
| SMILES | OB(O)C1=CC=C(C=C1)[N+]([O-])=O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|
AAH2776703
|
Thermo Scientific Chemicals
H2776703 |
1 g |
Each for $128.86
|
|
|||||
|
AAH2776706
|
Thermo Scientific Chemicals
H2776706 |
5 g |
Each for $400.73
|
|
|||||
Description
It is reagent used forligand-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 cyanation, 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. It is used in Preparation of combretastatin analogs as potential antitumor agents and human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsIt is reagent used forligand-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 cyanation, 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. It is used in Preparation of combretastatin analogs as potential antitumor agents and human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses
Solubility
Slightly soluble in water.
Notes
Store in cool dry conditions. Incompatible with oxidizing agents.
Chemical Identifiers
| 24067-17-2 | |
| 166.93 | |
| NSFJAFZHYOAMHL-UHFFFAOYSA-N | |
| 2773552 | |
| OB(O)C1=CC=C(C=C1)[N+]([O-])=O |
| C6H6BNO4 | |
| MFCD00161360 | |
| 4-nitrophenyl boronic acid, 4-nitrobenzeneboronic acid, p-nitrophenylboronic acid, 4-nitrophenylboronicacid, p-nitrophenyl boronic acid, 4-nitro phenyl boronic acid, boronic acid, 4-nitrophenyl, boronic acid, b-4-nitrophenyl, 4-borononitrobenzene | |
| (4-nitrophenyl)boronic acid |
Specifications
| 24067-17-2 | |
| C6H6BNO4 | |
| 1 g | |
| Slightly soluble in water. | |
| OB(O)C1=CC=C(C=C1)[N+]([O-])=O | |
| 166.93 | |
| 166.93 | |
| 4-Nitrobenzeneboronic acid |
| ∽285°C (decomposition) | |
| MFCD00161360 | |
| 4-nitrophenyl boronic acid, 4-nitrobenzeneboronic acid, p-nitrophenylboronic acid, 4-nitrophenylboronicacid, p-nitrophenyl boronic acid, 4-nitro phenyl boronic acid, boronic acid, 4-nitrophenyl, boronic acid, b-4-nitrophenyl, 4-borononitrobenzene | |
| NSFJAFZHYOAMHL-UHFFFAOYSA-N | |
| (4-nitrophenyl)boronic acid | |
| 2773552 | |
| 95% |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
H302-H315-H319-H335
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only