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About This Item
Linear Formula:
lC6H3(OH)CHO
CAS Number:
Molecular Weight:
248.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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’.
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Synthesis of 5-ortho-Carboranylsalicylaldehyde and an Indolinospirobenzopyran.
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An efficient and convenient synthesis of 5-formylsalicylaldehyde.
Lee SH, et al.
Synthetic Communications, 30(6), 1003-1008 (2000)
Synthesis and catalytic properties of p-acylthio (phenylacetylene) n substituted chiral manganese salen complexes.
Nielsen M and Gothelf KV.
Journal of the Chemical Society. Perkin Transactions 1, 19 (2001)
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