746177
MIBA
96%
Synonym(s):
5-Methoxy-2-iodophenylboronic acid
About This Item
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Quality Level
assay
96%
form
solid
greener alternative product characteristics
Catalysis
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Greener Alternative Product
mp
202-207 °C
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
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Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Research in the Hall Group is centered on organoboron chemistry and explores various applications of boronic acid derivatives in reaction development, catalysis, natural product synthesis, and chemical biology. Hall and his co-workers have pioneered the concept of "Boronic Acid Catalysis” (BAC), an emerging strategy for the direct activation of carboxylic acids and alcohols.
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