480096
2,6-Dimethoxyphenylboronic acid
≥97%
Synonym(s):
2,6-Dimethoxybenzeneboronic acid
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About This Item
Linear Formula:
(CH3O)2C6H3B(OH)2
CAS Number:
Molecular Weight:
181.98
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Product Name
2,6-Dimethoxyphenylboronic acid, ≥97%
InChI
1S/C8H11BO4/c1-12-6-4-3-5-7(13-2)8(6)9(10)11/h3-5,10-11H,1-2H3
SMILES string
COc1cccc(OC)c1B(O)O
InChI key
BKWVXPCYDRURMK-UHFFFAOYSA-N
assay
≥97%
mp
110-112 °C (lit.)
Quality Level
Related Categories
Application
2,6-Dimethoxyphenylboronic acid can be used as a reagent in:
- The palladium-catalyzed Suzuki-Miyaura coupling reaction to construct carbon-carbon bond.
- The synthesis of 2H-imidazo[1,5-a]pyridin-4-ium bromides, which are utilized as precursors for the preparation of N-heterocyclic carbene ligands.
- The preparation of monosubstituted benzothiazoloquinazolinones as potential monoamine oxidases inhibitors.
Reactant for:
- Suzuki-Miyaura reactions
Other Notes
Contains varying amounts of anhydride
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Imidazo [1, 5-a] pyridine-3-ylidenes-pyridine derived N-heterocyclic carbene ligands
Burstein, C, et al.
Tetrahedron, 61(26), 6207-6217 (2005)
Synthesis of 2-Aryl-12H-benzothiazolo [2, 3-b] quinazolin-12-ones and Their Activity Against Monoamine Oxidases
Jafari B, et al.
ChemistrySelect, 4(37), 11071-11076 (2019)
Palladium catalyzed Suzuki-Miyaura coupling with aryl chlorides using a bulky phenanthryl N-heterocyclic carbene ligand
Song C, et al.
Tetrahedron, 61(31), 7438-7446 (2005)
Ken T Ngo et al.
Journal of the American Chemical Society, 139(7), 2604-2618 (2017-01-25)
Electrocatalytic reduction of CO
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