Skip to Content
Merck
CN

283444

3,5-Diiodosalicylaldehyde

97%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
I2C6H2-2-(OH)CHO
CAS Number:
Molecular Weight:
373.91
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-117-2
MDL number:
Assay:
97%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

assay

97%

form

solid

mp

109-110 °C (lit.)

functional group

aldehyde, iodo

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

signalword

Warning

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

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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
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)



Global Trade Item Number

SKUGTIN
283444-5G04061826245859