746177
MIBA
96%
Synonym(s):
5-Methoxy-2-iodophenylboronic acid
About This Item
Recommended Products
Quality Level
Assay
96%
form
solid
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
202-207 °C
functional group
iodo
greener alternative category
, Aligned
storage temp.
2-8°C
SMILES string
OB(O)C1=C(I)C=CC(OC)=C1
InChI
1S/C7H8BIO3/c1-12-5-2-3-7(9)6(4-5)8(10)11/h2-4,10-11H,1H3
InChI key
XQYAEIDOJUNIGY-UHFFFAOYSA-N
General description
Application
Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect
Legal Information
related product
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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.
Customers Also Viewed
Related Content
Hall Group explores boronic acid derivatives' applications in reaction development and chemical biology.
Hall Group explores boronic acid derivatives' applications in reaction development and chemical biology.
Hall Group explores boronic acid derivatives' applications in reaction development and chemical biology.
Hall Group explores boronic acid derivatives' applications in reaction development and chemical biology.
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