추천 제품
vapor pressure
10 mmHg ( 656 °C)
Quality Level
grade
purum
분석
≥99.5%
반응 적합성
core: copper
reagent type: catalyst
mp
605 °C (lit.)
density
5.62 g/mL at 25 °C (lit.)
음이온 미량물
sulfate (SO42-): ≤5000 mg/kg
양이온 미량물
Fe: ≤50 mg/kg
SMILES string
[Cu+].[I-]
InChI
1S/Cu.HI/h;1H/q+1;/p-1
InChI key
LSXDOTMGLUJQCM-UHFFFAOYSA-M
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Copper(I) iodide, in combination with cesium fluoride, can be used to promote Stille coupling reaction. It can also mediate the reaction between arenethiolate ions and different
nonactivated aryl iodides in hexamethylphosphoric triamide to form aryl sulfides.
Copper(I) iodide can be used to catalyze:
nonactivated aryl iodides in hexamethylphosphoric triamide to form aryl sulfides.
Copper(I) iodide can be used to catalyze:
- Thioetherification of aryl halides using thiourea and alkyl bromides in wet polyethylene glycol and in the presence of potassium carbonate as a base.
- Reaction between acetylenes and metal halides in diethylamine to form transition metal alkynyl complexes.
- Reaction between terminal alkynes with phenylchalcogenyl halides to form alkynyl selenides, sulfides and tellurides.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT RE 1 Oral
표적 기관
Thyroid
Storage Class Code
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
이미 열람한 고객
Facile substitution reaction between nonactivated aryl iodides and arenethiolates in the presence of copper (I) iodide.
Chemistry Letters (Jpn), 9(11), 1363-1364 (1980)
Significant enhancement of the Stille reaction with a new combination of reagents?copper (I) iodide with cesium fluoride.
Chemistry?A European Journal, 11(11), 3294-3308 (2005)
One?Pot Thioetherification of Aryl Halides Using Thiourea and Alkyl Bromides Catalyzed by Copper (I) Iodide Free from Foul?Smelling Thiols in Wet Polyethylene Glycol (PEG 200).
Advanced Synthesis & Catalysis, 352(1), 119-124 (2010)
Convenient preparation of alkynyl selenides, sulfides and tellurides from terminal alkynes and prenylchalcogenyl halides in the presence of copper (I) iodide.
Tetrahedron Letters, 34(50), 8041-8042 (1993)
Novel preparation of σ-alkynyl complexes of transition metals by copper (I) iodide-catalysed dehydrohalogenation.
Journal of the Chemical Society. Chemical Communications, 9, 291-292 (1977)
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