4-Formylphenylboronic acid
ALDRICH/431966 - ≥95.0%
Synonym: 4-
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
assay | ≥95.0% |
InChI | 1S/C7H7BO3/c9-5-6-1-3-7(4 |
InChI key | VXWBQOJISHAKKM-UHFFFAOYSA |
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]are • 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 |
Symbol | GHS07 |
Signal word | Warning |
Hazard statements | H317 |
Precautionary statements | P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364 |
Hazard Codes | C |
Risk Statements | 34 |
Safety Statements | 22-26-36/37/39-45 |
RIDADR | NONH for all modes of transport |
WGK Germany | WGK 1 |
Purity | ≥95.0% |
mp | 237-242 °C (lit.) |
UNSPSC | 12352103 |