524328
5-Iodosalicylaldehyde
97%
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About This Item
Linear Formula:
lC6H3(OH)CHO
CAS Number:
Molecular Weight:
248.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
98-100 °C (lit.)
functional group
aldehyde, iodo
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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An efficient and convenient synthesis of 5-formylsalicylaldehyde.
Lee SH, et al.
Synthetic Communications, 30(6), 1003-1008 (2000)
Synthesis of 5-ortho-Carboranylsalicylaldehyde and an Indolinospirobenzopyran.
Lee SH, et al.
Synthetic Communications, 39(22), 4069-4078 (2009)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 524328-1G | 04061832549781 |