Basic information Safety Supplier Related

3,5-DICHLORO-4-HYDROXYBENZALDEHYDE

Basic information Safety Supplier Related

3,5-DICHLORO-4-HYDROXYBENZALDEHYDE Basic information

Product Name:
3,5-DICHLORO-4-HYDROXYBENZALDEHYDE
Synonyms:
  • 3,5-DICHLORO-4-HYDROXYBENZALDEHYDE
  • AKOS B029235
  • Benzaldehyde, 3,5-dichloro-4-hydroxy-
  • 2,6-Dichloro-4-formylphenol
  • Nipaguard DCHB 30
  • NSC 31590
  • 5-DICHLORO-4-HYDROXYBENZALDEHYDE
  • 3,5-Dichloro-4-hydroxybenzaldehyd
CAS:
2314-36-5
MF:
C7H4Cl2O2
MW:
191.01
Product Categories:
  • Aromatic Aldehydes & Derivatives (substituted)
  • Aldehydes
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
Mol File:
2314-36-5.mol
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3,5-DICHLORO-4-HYDROXYBENZALDEHYDE Chemical Properties

Melting point:
154 °C
Boiling point:
256.7±35.0 °C(Predicted)
Density 
1.547±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
4.85±0.23(Predicted)
color 
White
CAS DataBase Reference
2314-36-5
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
Hazard Note 
Irritant
HS Code 
2913000090
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3,5-DICHLORO-4-HYDROXYBENZALDEHYDE Usage And Synthesis

Uses

3,5-Dichloro-4-hydroxybenzaldehyde (cas# 2314-36-5) is a useful research chemical. It is used in fluorescent dye, preparation method therefor and use thereof.

Synthesis

2432-12-4

2314-36-5

General procedure for the synthesis of 3,5-dichloro-4-hydroxybenzaldehyde from 2,6-dichloro-4-methylphenol: A mixture of the substrate 2,6-dichloro-4-methylphenol (1 mmol), cobalt salts (n1 mol%), and NaOH (n2 equiv.) in ethylene glycol (5 mL) was subjected to a stirring reaction under an atmosphere of oxygen (1 atm) at 80°C for 8 hours. Upon completion of the reaction, hydrochloric acid (10 mL, 2%) and methyl tert-butyl ether (MTBE, 10 mL) were sequentially added to the reaction mixture. The organic layer was separated and the aqueous phase was further extracted with MTBE (10 mL x 2). All organic phases were combined, dried with anhydrous sodium sulfate and concentrated to obtain the residue. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 10:1, v/v) to afford the target product 3,5-dichloro-4-hydroxybenzaldehyde.

References

[1] Tetrahedron Letters, 2014, vol. 55, # 8, p. 1406 - 1411
[2] Green Chemistry, 2014, vol. 16, # 5, p. 2807 - 2814
[3] Green Chemistry, 2014, vol. 16, # 3, p. 1248 - 1254

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