499943
2-Benzofuranylboronic acid
≥95%
Synonym(s):
2-Benzofuranboronic acid, Benzofuran-2-ylboronic acid
About This Item
Recommended Products
![Benzo[b]thien-2-ylboronic acid ≥95%](/deepweb/assets/sigmaaldrich/product/structures/251/077/d0ead874-b533-4dcb-890d-8816a0018ccd/640/d0ead874-b533-4dcb-890d-8816a0018ccd.png)
Assay
≥95%
mp
114-116 °C (lit.)
SMILES string
OB(O)c1cc2ccccc2o1
InChI
1S/C8H7BO3/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5,10-11H
InChI key
PKRRNTJIHGOMRC-UHFFFAOYSA-N
Related Categories
Other Notes
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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.
Customers Also Viewed
Articles
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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