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4-Formylphenylboronic acid

ALDRICH/431966 - ≥95.0%

Synonym: 4-(Dihydroxyboryl)benzaldehyde; 4-Boronobenzaldehyde; 4-Formylbenzeneboronic acid; p-Formylbenzeneboronic acid; p-Formylphenylboronic acid

CAS Number: 87199-17-5
Empirical Formula (Hill Notation): C7H7BO3
Molecular Weight: 149.94
MDL Number: MFCD00151823
Linear Formula: HCOC6H4B(OH)2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-431966-1G 1 g
$36.50
1/EA
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45-431966-5G 5 g
$121.00
1/EA
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45-431966-25G 25 g
$313.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 431966-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 431966-5G

 

assay ≥95.0%
InChI 1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H
InChI key VXWBQOJISHAKKM-UHFFFAOYSA-N
mp 237-242 °C (lit.)
SMILES string OB(O)c1ccc(C=O)cc1
Application: 4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions and it can be used as a reagent for:
• Palladium-catalyzed 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.
• The synthesis of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells.
• The synthesis of a novel protein synthesis inhibitor active against Gram-positive bacteria.
• The Suzuki aryl-aryl coupling of the upper rim of hexahomotrioxacalix[3]arene.
• A rhodium-catalyzed cyclization, converting 1,5-enynes to cyclopentenes and spiro-cyclopentenes.
Other Notes: Contains varying amounts of anhydride
Packaging: 1, 5, 25 g in glass bottle
Purity ≥95.0%
mp 237-242 °C (lit.)
UNSPSC 12352103

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