1-Chloro-3-iodobenzene
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
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)
MSDS
- Language:English Provider:3-Chloroiodobenzene
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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