208221
Iodine monochloride
reagent grade, ≥95%
Synonym(s):
Chloroiodide
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About This Item
Linear Formula:
ICl
CAS Number:
Molecular Weight:
162.36
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352300
EC Number:
232-236-7
MDL number:
Assay:
≥95%
Grade:
reagent grade
Form:
solid or liquid
Product Name
Iodine monochloride, reagent grade, ≥95%
InChI key
QZRGKCOWNLSUDK-UHFFFAOYSA-N
InChI
1S/ClI/c1-2
SMILES string
ClI
grade
reagent grade
assay
≥95%
form
solid or liquid
bp
97.4 °C (lit.)
density
3.24 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
Iodine monochloride (ICl) may be employed as a reagent in the following processes:
- Halogenation of methoxy and dimethoxybenzenes
- Synthesis of flavones.
- Preparation of 1-naphthaldehydes.
General description
Iodine monochloride is an interhalogen compound. It forms various complexes with ethyl, isopropyl and t-butylbenzenes. Electrically conducting solution of ICl is obtained on dissolution of ICl in polar solvents. ICl is a green oxidizing agent and participates in the following transformations:
- aldose hemiacetals to the corresponding aldose lactones
- diarylmethanols to the corresponding diarylmethanones
- arylalkylmethanols to the corresponding arylalkylmethanones
- dialkylmethanols to the corresponding dialkylmethanones
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
危险化学品
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Synthesis of 1-naphthaldehydes via the cascade reactions of 1-phenylpent-4-yn-2-ols promoted by iodine monochloride
Li B, et al.
Tetrahedron Letters, 57.17, 1843-1846 (2016)
Iodine Monochloride (ICl) as a Highly Efficient, Green Oxidant for the Oxidation of Alcohols to Corresponding Carbonyl Compounds
Wei, Peng, et al.
Synthetic Communications, 45.12, 1457-1470 (2015)
A mild and convenient procedure for conversion of alkenes into alkyl iodides via reaction of iodine monochloride with organoboranes.
Kabalka GW and Gooch III EE.
The Journal of Organic Chemistry, 45(18), 3578-3580 (1980)
Polymethylbenzene complexes of iodine and iodine monochloride.
Andrews LJ and Keefer RM.
Journal of the American Chemical Society, 74(18), 4500-4503 (1952)
Ultrasonic-assisted synthesis of flavones by oxidative cyclization of 2'-hydroxychalcones using iodine monochloride.
Lahyani A and Trabelsi M.
Ultrasonics Sonochemistry, 31, 626-630 (2016)
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