Basic information Safety Supplier Related

3,5-DIIODO-4-HYDROXYBENZALDEHYDE

Basic information Safety Supplier Related

3,5-DIIODO-4-HYDROXYBENZALDEHYDE Basic information

Product Name:
3,5-DIIODO-4-HYDROXYBENZALDEHYDE
Synonyms:
  • AKOS B028744
  • 3,5-DIIODO-4-HYDROXYBENZALDEHYDE
  • 4-HYDROXY-3,5-DIIODO-BENZALDEHYDE
  • 3,5-Diiodo-4-Hydroxybenzaldhyde
  • 3,5-DIIODO-4-HYDROXYBENZALDEHYDE, 98+%
  • Levothyroxine Sodium Impurity f
  • 2,6-Diiodo-4-formylphenol
  • NSC 72943
CAS:
1948-40-9
MF:
C7H4I2O2
MW:
373.91
EINECS:
217-754-3
Product Categories:
  • Aromatic Aldehydes & Derivatives (substituted)
  • Aromatics
  • Miscellaneous Reagents
Mol File:
1948-40-9.mol
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3,5-DIIODO-4-HYDROXYBENZALDEHYDE Chemical Properties

Melting point:
202-203°C
Boiling point:
284.1±40.0 °C(Predicted)
Density 
2.602±0.06 g/cm3(Predicted)
storage temp. 
-20°C Freezer, Under Inert Atmosphere
solubility 
Chloroform (Slightly, Sonicated), DMSO (Slightly)
form 
Solid
pka
4.89±0.23(Predicted)
color 
White to Pale Yellow
Water Solubility 
Insoluble in water. Sparingly soluble in chloroform and methanol.
Sensitive 
Air & Light Sensitive
BRN 
1283414
InChI
InChI=1S/C7H4I2O2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H
InChIKey
WHLUEIMENHLCMY-UHFFFAOYSA-N
SMILES
C(=O)C1=CC(I)=C(O)C(I)=C1
CAS DataBase Reference
1948-40-9(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
HS Code 
2913000090

MSDS

  • Language:English Provider:ALFA
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3,5-DIIODO-4-HYDROXYBENZALDEHYDE Usage And Synthesis

Chemical Properties

Pale Beige Solid

Uses

3,5-Diiodo-4-hydroxybenzaldehyde (cas# 1948-40-9) is a compound useful in organic synthesis.

Synthesis

3,5-Diiodo-4-hydroxybenzaldehyde was prepared as follows: in a 100 mL round bottom flask, 4-hydroxybenzaldehyde (1.0 g, 8.19 mmol), sodium periodate (1.75 g, 8.19 mmol), and NaCl (957 mg, 16.38 mmol) were dissolved in acetic acid (30 mL). H2O (3 mL) was added at room temperature. The reaction mixture was stirred at room temperature for 10 min, then potassium iodide (2.72 g, 16.4 mmol) was added and the reaction mixture was stirred at room temperature for 96 hours. The reaction mixture was diluted with EtOAc (25 mL) and 1 M aqueous sodium thiosulfate. The solution (25 mL) was added and the resulting mixture was stirred for 15 minutes. The solution was poured into 250 mLErlenmeyer and washed with EtOAc (50 mL) and 1 M aqueous sodium thiosulfate. solution (50mL) and the resulting solution was stirred for another 15 minutes. The organic layer was separated and the aqueous phase was further extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated to dryness to afford 4-hydroxy-3,5-diiodobenzaldehyde (2.91 g, 95% yield) as a light yellow solid.

3,5-DIIODO-4-HYDROXYBENZALDEHYDESupplier

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