Assay
97%
mp
98-100 °C (lit.)
SMILES string
Oc1ccc(I)cc1C=O
InChI
1S/C7H5IO2/c8-6-1-2-7(10)5(3-6)4-9/h1-4,10H
InChI key
PDFVIWFKGYODKD-UHFFFAOYSA-N
General description
5-Iodosalicylaldehyde is a salicylaldehyde derivative.
Application
5-Iodosalicylaldehyde may be used to synthesize:
- 5-formylsalicylaldehyde
- 5-ortho-carboranylsalicylaldehyde
- new salen (N,N′-Bis(salicylidene)ethylenediamine) ligands that are tethered to a p-acylthio(phenylacetylene)n linker
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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
Synthesis of 5-ortho-Carboranylsalicylaldehyde and an Indolinospirobenzopyran.
Synthetic Communications, 39(22), 4069-4078 (2009)
Synthesis and catalytic properties of p-acylthio (phenylacetylene) n substituted chiral manganese salen complexes.
Journal of the Chemical Society. Perkin Transactions 1, 19 (2001)
An efficient and convenient synthesis of 5-formylsalicylaldehyde.
Synthetic Communications, 30(6), 1003-1008 (2000)
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