About This Item
Recommended Products
![[Bis(trifluoroacetoxy)iodo]benzene 97%](/deepweb/assets/sigmaaldrich/product/structures/238/293/71fcde9a-4afb-4cf5-9c22-8d8d68bf1ba4/640/71fcde9a-4afb-4cf5-9c22-8d8d68bf1ba4.png)
form
solid
reaction suitability
reaction type: C-C Bond Formation
storage temp.
−20°C
Application
Automate your fluorination reactions with Synple Automated Synthesis Platform (SYNPLE-SC002)
Legal Information
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:
Certificates of Analysis (COA)
Sorry, we don't have COAs for this product available online at this time.
If you need assistance, please contact Customer Support.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Fluoroalkylation toolbox expands with various reagents for late-stage fluoroalkylation in organic synthesis and medicinal chemistry.
Fluoroalkylation toolbox expands with various reagents for late-stage fluoroalkylation in organic synthesis and medicinal chemistry.
Fluoroalkylation toolbox expands with various reagents for late-stage fluoroalkylation in organic synthesis and medicinal chemistry.
Fluoroalkylation toolbox expands with various reagents for late-stage fluoroalkylation in organic synthesis and medicinal chemistry.
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