추천 제품
Grade
ACS reagent
vapor density
>1 (vs air)
분석
≥99.0%
형태
crystalline powder
crystals or granules
반응 적합성
reagent type: catalyst
core: copper
불순물
≤0.01% insolubles
mp
100 °C (dec.) (lit.)
음이온 미량물
nitrate (NO3-): ≤0.015%
sulfate (SO42-): ≤0.005%
양이온 미량물
Ca: ≤0.005%
Fe: ≤0.005%
K: ≤0.01%
Na: ≤0.02%
Ni: ≤0.01%
SMILES string
Cl[Cu]Cl.[H]O[H].[H]O[H]
InChI
1S/2ClH.Cu.2H2O/h2*1H;;2*1H2/q;;+2;;/p-2
InChI key
MPTQRFCYZCXJFQ-UHFFFAOYSA-L
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Copper(II) chloride dihydrate can be used as a catalyst:
- For the conversion of dimedone into N-arylhydrazinecarbothioamide based indazole derivatives by reacting with phenylhydrazine, hydrazine hydrate, and substituted arylisothiocyanates.
- In the three-component Domino reaction ofarylboronic acids, arylcyanamides, and amines to synthesize 2-aminobenzimidazoles in the presence of bipyridine ligand.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2
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)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Deprotection of t-butyldimethylsiloxy (TBDMS) protecting group with catalytic copper (II) chloride dihydrate.
TAN ZP, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 11(9), 753-756 (2000)
An X-ray refinement of the crystal structure of copper (II) chloride dihydrate.
Engberg ?.
Acta Chemica Scandinavica, 24(10), 6-6 (1970)
Interaction of hydrazine with copper (II) chloride in acidic solutions. Formation, spectral and magnetic properties, and structures of copper (II), copper (I), and mixed-valence species.
Brown DB, et al.
Inorganic Chemistry, 18(10), 2635-2641 (1979)
Regeneration of carbonyl compounds from semicarbazones by copper (II) chloride dihydrate.
Ram RN and Varsha K.
Tetrahedron Letters, 32(41), 5829-5832 (1991)
Kenji Funaki et al.
Organic letters, 14(24), 6186-6189 (2012-12-12)
Direct arylation of thiophenes and benzothiophenes with aryltrimethylsilanes was effectively catalyzed by PdCl(2)(MeCN)(2) in the presence of CuCl(2) as an oxidant. The reaction preferentially occurred at the β-position of both thiophenes and benzothiophenes.
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