- 4-Nitrophenylboronic acid
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- $100.00 / 1KG
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2023-12-26
- CAS:24067-17-2
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 4-Nitrophenylboronic acid Basic information |
| | 4-Nitrophenylboronic acid Chemical Properties |
| Melting point | 285-290°C (dec.) | | Boiling point | 373.7±44.0 °C(Predicted) | | density | 1.40±0.1 g/cm3(Predicted) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | DMF: 15 mg/ml; DMSO: 15 mg/ml; Ethanol: 15 mg/ml; Ethanol:PBS (pH 7.2) (1:5): 0.16 mg/ml | | pka | 7.04±0.10(Predicted) | | form | Crystalline Powder | | color | White to yellow | | Water Solubility | Slightly soluble in water. | | InChIKey | NSFJAFZHYOAMHL-UHFFFAOYSA-N | | CAS DataBase Reference | 24067-17-2(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 22 | | Safety Statements | 26-36/37/39-24/25 | | WGK Germany | 3 | | Hazard Note | Harmful | | HS Code | 29319090 |
| | 4-Nitrophenylboronic acid Usage And Synthesis |
| Description | 4-Nitrobenzeneboronic acid is an arylboronic acid building block that has been used in the synthesis of phenols. | | Chemical Properties | White to brown powder or crystal | | Uses | Reagent used for
- 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
| | Uses | suzuki reaction | | Uses | 4-Nitrophenylboronic Acid is a useful synthetic intermediate. It is a reagent used for ligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings, Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines and Diels-Alder or C-H activation reactions. |
| | 4-Nitrophenylboronic acid Preparation Products And Raw materials |
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