Skip to Content
MilliporeSigma
All Photos(2)

Documents

480096

Sigma-Aldrich

2,6-Dimethoxyphenylboronic acid

≥97%

Synonym(s):

2,6-Dimethoxybenzeneboronic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3O)2C6H3B(OH)2
CAS Number:
Molecular Weight:
181.98
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

assay

≥97%

mp

110-112 °C (lit.)

SMILES string

COc1cccc(OC)c1B(O)O

InChI

1S/C8H11BO4/c1-12-6-4-3-5-7(13-2)8(6)9(10)11/h3-5,10-11H,1-2H3

InChI key

BKWVXPCYDRURMK-UHFFFAOYSA-N

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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)
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)
Ken T Ngo et al.
Journal of the American Chemical Society, 139(7), 2604-2618 (2017-01-25)
Electrocatalytic reduction of CO

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service