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1-Chloro-3-iodobenzene

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1-Chloro-3-iodobenzene Basic information

Product Name:
1-Chloro-3-iodobenzene
Synonyms:
  • 1-Chloro-3-iodobenzene, 98% clear colourless to pale yellow or pale pink liquid
  • oroiodobenzene
  • 1-chloro-3-iodo-benzen
  • 3-Chloro-1-iodobenzene
  • 3-Iodochlorobenzene
  • m-Chlorophenyl iodide
  • M-CHLOROIODOBENZENE
  • 3-CHLOROIODOBENZENE
CAS:
625-99-0
MF:
C6H4ClI
MW:
238.45
EINECS:
210-920-6
Product Categories:
  • alkyl Iodine| alkyl chloride
  • Aromatic Halides (substituted)
  • Chlorine Compounds
  • Iodine Compounds
  • Aryl
  • Halogenated Hydrocarbons
  • C6
Mol File:
625-99-0.mol
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1-Chloro-3-iodobenzene Chemical Properties

Melting point:
95-96 °C
Boiling point:
103-104 °C15 mm Hg(lit.)
Density 
1.926 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.631(lit.)
Flash point:
215 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Liquid
Specific Gravity
1.926
color 
Clear light yellow
Water Solubility 
Soluble in water 67.2 mg/L.
Sensitive 
Light Sensitive
BRN 
1904539
CAS DataBase Reference
625-99-0(CAS DataBase Reference)
NIST Chemistry Reference
Benzene, 1-chloro-3-iodo-(625-99-0)
EPA Substance Registry System
Benzene, 1-chloro-3-iodo- (625-99-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25
WGK Germany 
3
TSCA 
T
HazardClass 
IRRITANT
HS Code 
29039990

MSDS

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1-Chloro-3-iodobenzene Usage And Synthesis

Chemical Properties

Clear light yellow liquid

Uses

suzuki reaction

Uses

1-Chloro-3-iodobenzene is used as a pharmaceutical intermediate.

Synthesis Reference(s)

Synthetic Communications, 11, p. 639, 1981 DOI: 10.1080/00397918108063637

General Description

The multiple-quantum proton NMR spectra of 3-chloroiodobenzene was studied.

Synthesis

63503-60-6

625-99-0

General procedure for the synthesis of m-chloroiodobenzene from 3-chlorophenylboronic acid: a mixture of arylboronic acid (0.55 mmol), KF (96 mg, 1.65 mmol) and I2 (127 mg, 0.50 mmol) in 1,4-dioxane (5 mL) was stirred and reacted for 1 hr at 80 °C. After completion of the reaction, the mixture was filtered through a silica gel column and eluted with ether (10 mL). Subsequently, the solvent was removed by rotary evaporator. For further purification, the target product, m-chloroiodobenzene, was isolated by silica gel column chromatography using petroleum ether/ether (98:2) as eluent.

References

[1] Chemistry - A European Journal, 2011, vol. 17, # 20, p. 5652 - 5660
[2] Tetrahedron Letters, 2015, vol. 56, # 9, p. 1122 - 1123
[3] Synlett, 1998, # 2, p. 141 - 142
[4] Synlett, 2014, vol. 25, # 7, p. 995 - 1000

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