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4-Formylbenzeneboronic acid, 97%
CAS: 87199-17-5 | C7H7BO3 | 149.94 g/mol
Supplier: Thermo Scientific Chemicals B2519903
Description
4-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.
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.
Applications4-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.
Solubility
Slightly Soluble in water.
Notes
Air Sensitive. Store away from air and oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Specifications
| 4-Formylbenzeneboronic acid | |
| 260°C to 266°C | |
| MFCD00151823 | |
| 3030770 | |
| 4-formylphenyl boronic acid, 4-formylbenzeneboronic acid, 4-boronobenzaldehyde, boronic acid, 4-formylphenyl, boronic acid, b-4-formylphenyl, p-formylphenylboronic acid, 4-dihydroxyboryl benzaldehyde, 4-dihydroxyboranyl benzaldehyde, 4-benzaldehyde boronic acid, 4-formyl-phenylboronic acid | |
| VXWBQOJISHAKKM-UHFFFAOYSA-N | |
| (4-formylphenyl)boronic acid | |
| 591073 | |
| 97% |
| 87199-17-5 | |
| C7H7BO3 | |
| 1 g | |
| Air Sensitive | |
| Slightly Soluble in water. | |
| OB(O)C1=CC=C(C=O)C=C1 | |
| 149.94 | |
| 149.94 |
Chemical Identifiers
| 87199-17-5 | |
| 149.94 | |
| VXWBQOJISHAKKM-UHFFFAOYSA-N | |
| 591073 | |
| OB(O)C1=CC=C(C=O)C=C1 |
| C7H7BO3 | |
| MFCD00151823 | |
| 4-formylphenyl boronic acid, 4-formylbenzeneboronic acid, 4-boronobenzaldehyde, boronic acid, 4-formylphenyl, boronic acid, b-4-formylphenyl, p-formylphenylboronic acid, 4-dihydroxyboryl benzaldehyde, 4-dihydroxyboranyl benzaldehyde, 4-benzaldehyde boronic acid, 4-formyl-phenylboronic acid | |
| (4-formylphenyl)boronic acid |
Safety and Handling
GHS H Statement
H317
May cause an allergic skin reaction.
P261-P272-P280g-P302+P352-P333+P313-P363-P501c
H317
EINECSNumber : 438-670-5
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only