ChemicalBook > CAS DataBase List > 4-chloro-3-iodobenzaldehyde

4-chloro-3-iodobenzaldehyde

Product Name
4-chloro-3-iodobenzaldehyde
CAS No.
276866-90-1
Chemical Name
4-chloro-3-iodobenzaldehyde
Synonyms
4-chloro-3-iodobenzaldehyde;4-dhloro-3-iodobenzaldehyde;Benzaldehyde, 4-chloro-3-iodo-
CBNumber
CB51559467
Molecular Formula
C7H4ClIO
Formula Weight
266.46
MOL File
276866-90-1.mol
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4-chloro-3-iodobenzaldehyde Property

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
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Safety

HS Code 
2913000090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Ark Pharm
Product number
AK177782
Product name
4-Chloro-3-iodobenzaldehyde
Purity
95+%
Packaging
1g
Price
$119
Updated
2021/12/16
SynQuest Laboratories
Product number
2615-M-06
Product name
4-Chloro-3-iodobenzaldehyde
Packaging
250mg
Price
$157
Updated
2021/12/16
AK Scientific
Product number
5972CS
Product name
4-Chloro-3-iodobenzaldehyde
Packaging
250mg
Price
$242
Updated
2021/12/16
SynQuest Laboratories
Product number
2615-M-06
Product name
4-Chloro-3-iodobenzaldehyde
Packaging
1g
Price
$336
Updated
2021/12/16
AK Scientific
Product number
5972CS
Product name
4-Chloro-3-iodobenzaldehyde
Packaging
5g
Price
$1327
Updated
2021/12/16
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4-chloro-3-iodobenzaldehyde Chemical Properties,Usage,Production

Synthesis

104-88-1

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

4-chloro-3-iodobenzaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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276866-90-1, 4-chloro-3-iodobenzaldehydeRelated Search:


  • 4-chloro-3-iodobenzaldehyde
  • Benzaldehyde, 4-chloro-3-iodo-
  • 4-dhloro-3-iodobenzaldehyde
  • 276866-90-1