Learn More
4-Nitrobenzeneboronic acid, 95%, Thermo Scientific Chemicals
64.40 € - 212.00 €
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 |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
---|---|---|---|---|---|---|---|---|---|
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
11312939
|
Thermo Scientific Alfa Aesar
H27767.03 |
1 g |
64.40 €
1g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
11322939
|
Thermo Scientific Alfa Aesar
H27767.06 |
5 g |
212.00 €
5g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
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 | |
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% |
∽285°C (decomposition) | |
MFCD00161360 | |
Slightly soluble in water. | |
OB(O)C1=CC=C(C=C1)[N+]([O-])=O | |
166.93 | |
166.93 | |
4-Nitrobenzeneboronic acid |
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
missing translation for 'tsca' : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only
Your input is important to us. Please complete this form to provide feedback related to the content on this product.