393622
p-Tolylboronic acid
97%
Sinónimos:
(p-Methylphenyl)boronic acid, 4-Methylbenzeneboronic acid, 4-Methylphenylboronic acid, 4-Tolueneboronic acid, 4-Tolylboronic acid, p-Tolueneboronic acid, NSC 62870, p-Methylbenzeneboronic acid
About This Item
Productos recomendados
Quality Level
assay
97%
mp
256-263 °C (lit.)
SMILES string
Cc1ccc(cc1)B(O)O
InChI
1S/C7H9BO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5,9-10H,1H3
InChI key
BIWQNIMLAISTBV-UHFFFAOYSA-N
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Application
- Palladium (Pd)-catalyzed direct arylation[1]
- Direct Palladium(II)-Catalyzed Synthesis[2]
- Palladium-catalyzed arylation by Suzuki-Miyaura cross-coupling in water[3]
- Cyclopalladation[4]
- Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence[5]
- Ruthenium catalyzed direct arylation[6]
- Rhodium-catalyzed asymmetric conjugate addition[7]
- Ligand-free copper-catalyzed cross-coupling reactions[8]
- Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions[9]
- Ligand-free Suzuki, Sonogashira, and Heck cross-coupling reactions[10]
Reagent used in Preparation of
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Artículos
MIDA-protected boronate esters offer stability, chromatography compatibility, and reactivity in anhydrous cross-coupling conditions.
MIDA-protected boronate esters offer stability, chromatography compatibility, and reactivity in anhydrous cross-coupling conditions.
MIDA-protected boronate esters offer stability, chromatography compatibility, and reactivity in anhydrous cross-coupling conditions.
MIDA-protected boronate esters offer stability, chromatography compatibility, and reactivity in anhydrous cross-coupling conditions.
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