722057
4′-Hydroxy-3′-iodoacetophenone
97%
Synonym(s):
1-(4-Hydroxy-3-iodophenyl)ethanone, 2-Iodo-4-acetylphenol, 3-Iodo-4-hydroxyacetophenone, 4-Acetyl-2-iodophenol
About This Item
Recommended Products
Quality Level
Assay
97%
form
powder
mp
155-160 °C
SMILES string
CC(=O)c1ccc(O)c(I)c1
InChI
1S/C8H7IO2/c1-5(10)6-2-3-8(11)7(9)4-6/h2-4,11H,1H3
InChI key
SJRAJHOOMLHHQN-UHFFFAOYSA-N
Related Categories
Application
- Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenes
- Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction
- Regioselective synthesis of indene derivatives via Pd/C-catalyzed cyclization reaction in air
- Preparation of carbazoles via cross-coupling with silylaryl triflates followed by palladium-catalyzed cyclization
- Stereoselective preparation of heteropolycyclic compounds via palladium-catalyzed stereoselective heteroannulation of with cyclic alkenes
- Preparation of disubstituted coumarins via palladium-catalyzed carbonylative annulation of internal alkynes
- Preparation of arylalkynes, benzofurans and indoles via Sonogashira coupling and cyclization on alumina
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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
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