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480118

Sigma-Aldrich

3,4-Dimethoxyphenylboronic acid

≥95.0%

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About This Item

Linear Formula:
(CH3O)2C6H3B(OH)2
CAS Number:
122775-35-3
Molecular Weight:
181.98
MDL number:
MFCD01074574
UNSPSC Code:
12352103
PubChem Substance ID:
24871548
NACRES:
NA.22
Pricing and availability is not currently available.

assay

≥95.0%

mp

245-250 °C (lit.)

SMILES string

COc1ccc(cc1OC)B(O)O

InChI

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

InChI key

RCVDPBFUMYUKPB-UHFFFAOYSA-N

Application

3,4-Dimethoxyphenylboronic acid can be used:
  • As a substrate in the cross-coupling reaction with 5,7-dichloropyrido[4,3-d]pyrimidine catalyzed by palladium.[1]
  • As a starting material for the synthesis of buflavine 1, a natural alkaloid.[2]
  • In one of the key synthetic steps for the preparation of lipidated malarial glycosylphosphatidylinositols (GPI) disaccharide.[3]
  • To prepare 3,3″,4,4″-tetramethoxy-1,1′:4′,1″-terphenyl by reacting with 1,4-dibromobenzene using Pd catalyst.[4]

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)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS6492
MKCQ1873
MKCF7124
MKBX8820V
MKBS4054V

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3, 3″, 4, 4″-Tetramethoxy-1, 1′: 4′, 1″-terphenyl
Pui L, et al.
Acta Crystallographica Section E, Structure Reports Online, 67(Pt 8), o1892-o1892 (2011)
A Suzuki-Miyaura coupling mediated deprotection as key to the synthesis of a fully lipidated malarial GPI disaccharide
Liu X and Seeberger PH
Chemical Communications (Cambridge, England), 15, 1708-1709 (2004)
Highly efficient synthesis of buflavine: a unique Amaryllidaceae alkaloid
Sahakitpichan P and Ruchirawat S
Tetrahedron Letters, 44(28), 5239-5241 (2003)
Regioselective cross-coupling reactions and nucleophilic aromatic substitutions on a 5, 7-dichloropyrido [4, 3-d] pyrimidine scaffold
Jang M, et al.
Tetrahedron Letters, 47(50), 8917-8920 (2006)

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