480118
3,4-Dimethoxyphenylboronic acid
≥95.0%
Sign In to View Organizational & Contract Pricing.
Select a Size
5 G
$52.70
25 G
$98.30
$52.70
Available to ship TODAYDetails
Subscriptions are currently unavailable.
Ships Every 4 weeks
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:
Skip To
InChI
1S/C8H11BO4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5,10-11H,1-2H3
SMILES string
COc1ccc(cc1OC)B(O)O
InChI key
RCVDPBFUMYUKPB-UHFFFAOYSA-N
assay
≥95.0%
mp
245-250 °C (lit.)
Quality Level
Related Categories
1 of 4
This Item | 483451 | 512117 | 470317 |
|---|---|---|---|
| assay ≥95.0% | assay ≥95.0% | assay ≥95.0% | assay ≥95.0% |
| mp 245-250 °C (lit.) | mp 232-245 °C (lit.) | mp 225-230 °C (lit.) | mp 250 °C (dec.) (lit.) |
| Quality Level 100 | Quality Level 200 | Quality Level 100 | Quality Level 100 |
![Benzo[b]thien-3-ylboronic acid ≥95.0%](/deepweb/assets/sigmaaldrich/product/structures/136/961/9ddc053e-3519-47d3-be03-95715d131635/640/9ddc053e-3519-47d3-be03-95715d131635.png)
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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)
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)
Related Content
Active Filters
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