518786
4-Hydroxy-3-methoxyphenylboronic acid pinacol ester
98%
Synonym(s):
2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, 4-Hydroxy-3-methoxyphenylboronic acid, pinacol cyclic ester
About This Item
Recommended Products
![1-Methyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyridin-2-one AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/561/839/d79f546e-0338-46d4-abc1-b21eef32524e/640/d79f546e-0338-46d4-abc1-b21eef32524e.png)
![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)
Quality Level
assay
98%
mp
105-109 °C (lit.)
SMILES string
COc1cc(ccc1O)B2OC(C)(C)C(C)(C)O2
InChI
1S/C13H19BO4/c1-12(2)13(3,4)18-14(17-12)9-6-7-10(15)11(8-9)16-5/h6-8,15H,1-5H3
InChI key
WFSJROCEOJANPD-UHFFFAOYSA-N
Related Categories
Application
- In the Suzuki-Miyaura cross-coupling reaction.
- To prepare ethylidenedihydroindolones as potential neoplastic agents.
- To synthesize 5,6-dihydropyrrolo[2,1-b]isoquinoline derivatives, which can be utilized as scaffolds to prepare lamellarin analogs via regioselective bromination and Suzuki cross-coupling reactions.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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
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.
Articles
The synthesis of biaryl compounds via the Suzuki coupling reaction has become more commonplace now that many arylboronic acids are readily available. We are pleased to offer arylboronic acid pinacol esters4 as part of a growing line of products used in the Suzuki coupling reaction.
The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.
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