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Merck
모든 사진(3)

Key Documents

208221

Sigma-Aldrich

Iodine monochloride

reagent grade, ≥95%

동의어(들):

Chloroiodide

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About This Item

Linear Formula:
ICl
CAS Number:
Molecular Weight:
162.36
EC Number:
MDL number:
UNSPSC 코드:
12352300
PubChem Substance ID:
NACRES:
NA.21

Grade

reagent grade

Quality Level

분석

≥95%

형태

solid or liquid

bp

97.4 °C (lit.)

density

3.24 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

ClI

InChI

1S/ClI/c1-2

InChI key

QZRGKCOWNLSUDK-UHFFFAOYSA-N

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관련 카테고리

일반 설명

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

애플리케이션

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.
It may be used as an iodinating agent in the conversion of alkylboranes to alkyl iodides.

픽토그램

CorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

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)
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)
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)
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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