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283444

Sigma-Aldrich

3,5-Diiodosalicylaldehyde

97%

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About This Item

Fórmula lineal:
I2C6H2-2-(OH)CHO
Número de CAS:
2631-77-8
Peso molecular:
373.91
EC Number:
220-117-2
MDL number:
MFCD00003321
UNSPSC Code:
12352100
PubChem Substance ID:
24857104
NACRES:
NA.22

assay

97%

form

solid

mp

109-110 °C (lit.)

SMILES string

Oc1c(I)cc(I)cc1C=O

InChI

1S/C7H4I2O2/c8-5-1-4(3-10)7(11)6(9)2-5/h1-3,11H

InChI key

MYWSBJKVOUZCIA-UHFFFAOYSA-N

Application

3,5-Diiodosalicylaldehyde has been used in the synthesis of:
  • new Schiff bases, (2,4-diiodo-6-[(2-morpholin-4-yl-ethylimino)-methyl]-phenol and 2,4-diiodo-6-[(3-morpholin-4-yl-propylimino)-methyl]-phenol)
  • new tridentate ligand, [(2-hydroxy-3,5-diiodo-benzylidene)-amino]-acetic acid (HDBA)
  • 3-bromo-N′-(2-hydroxy-3,5-diiodobenzylidene)benzohydrazide monohydrate

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

225681

4-(Diethylamino)salicylaldehyde

Synthesis and antibacterial activities of copper (II) with [(2-hydroxy-3, 5-diiodo-benzylidene)-amino]-acetic acid.
Xu S-P, et al.
Journal of Coordination Chemistry, 63(19), 3463-3470 (2010)
Ganesan Jeya Shree et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 226, 117613-117613 (2019-10-14)
In this work, we designed a novel Schiff-base probe from the condensation reaction of 3,5-diiodosalicylaldehyde with isoniazid. Treatment of the sensor molecule with different metal ions like K+, Ba2+, Ca2+, Mg2+, Fe2+, Mn2+, Co2+, Cu2+, Cd2+, Ni2+, Hg2+, Zn2+, Pb2+
Synthesis and antibacterial activities of metal (II) complexes with Schiff bases derived from 3, 5-diiodosalicylaldehyde.
Xu S-P, et al.
Journal of Coordination Chemistry, 62(12), 2048-2057 (2009)
Jing-Heng Ning et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 4), o905-o906 (2009-01-01)
Crystals of the title compound, C(14)H(9)BrI(2)N(2)O(2)·H(2)O, were obtained from a condensation reaction of 3-bromo-benzohydrazide with 3,5-diiodo-salicylaldehyde. The Schiff base mol-ecule assumes an E configuration with respect to the C=N bond, and the dihedral angle between the two benzene rings is
Yang Pan et al.
Chemosphere, 144, 2312-2320 (2015-11-26)
During drinking water disinfection, iodinated disinfection byproducts (I-DBPs) can be generated through reactions between iodide, disinfectants, and natural organic matter. Drinking water I-DBPs have been increasingly attracting attention as emerging organic pollutants as a result of their significantly higher toxicity

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