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ChemicalBook--->CAS DataBase List--->276866-90-1

276866-90-1

276866-90-1 Structure

276866-90-1 Structure
IdentificationBack Directory
[Name]

4-chloro-3-iodobenzaldehyde
[CAS]

276866-90-1
[Synonyms]

4-chloro-3-iodobenzaldehyde
4-dhloro-3-iodobenzaldehyde
Benzaldehyde, 4-chloro-3-iodo-
[Molecular Formula]

C7H4ClIO
[MDL Number]

MFCD09836681
[MOL File]

276866-90-1.mol
[Molecular Weight]

266.46
Chemical PropertiesBack Directory
[Melting point ]

117 °C
[Boiling point ]

304.0±27.0 °C(Predicted)
[density ]

1.971±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2913000090
Spectrum DetailBack Directory
[Spectrum Detail]

4-chloro-3-iodobenzaldehyde(276866-90-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Chlorobenzaldehyde

104-88-1

4-chloro-3-iodobenzaldehyde

276866-90-1

The general procedure for the synthesis of 3-iodo-4-chlorobenzaldehyde from 4-chlorobenzaldehyde was as follows: iodine (1.12 g, 4.4 mmol) and sodium iodate (400 mg, 2.2 mmol) were added to a reaction vessel containing sulphuric acid (30 ml), and stirred at room temperature for 30 minutes. Subsequently, 4-chlorobenzaldehyde (1.40 g, 10.0 mmol) was added to the reaction mixture and stirring was continued for 1 hour at room temperature. After completion of the reaction, the reaction mixture was poured into ice water and the resulting solid was separated by filtration. After washing the solid with water to neutral, the solid was dissolved in ethanol and recrystallized to give 1.06 g (4.00 mmol, 40% yield) of 3-iodo-4-chlorobenzaldehyde.

[References]

[1] Bulletin of the Chemical Society of Japan, 2000, vol. 73, # 4, p. 951 - 956
[2] Tetrahedron, 2004, vol. 60, # 41, p. 9113 - 9119
[3] Synthesis, 2006, # 7, p. 1195 - 1199
[4] Patent: KR2016/149561, 2016, A. Location in patent: Paragraph 0125; 0126; 0127
[5] European Journal of Medicinal Chemistry, 2016, vol. 123, p. 180 - 190
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