추천 제품
Grade
reagent
vapor pressure
1.3 mmHg ( 236 °C)
제품 라인
ReagentPlus®
분석
99%
양식
powder
반응 적합성
reagent type: catalyst
core: mercury
mp
277 °C (lit.)
SMILES string
Cl[Hg]Cl
InChI
1S/2ClH.Hg/h2*1H;/q;;+2/p-2
InChI key
LWJROJCJINYWOX-UHFFFAOYSA-L
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일반 설명
Mercury(II) chloride is an inorganic salt with the molecular formula HgCl2. Its vapor phase Raman spectra has been recorded and analyzed. The molecular structure of HgCl2 has been investigated based on the electron diffraction analysis data. The effect of strong acids on its stretching vibration frequencies has been studied.
애플리케이션
Mercury(II) chloride (HgCl2) has been used in a study to understand its toxic impact on rat cortical neurons.
It may be used as a catalyst for the addition reaction between aromatic amines and terminal acetylenes. It may also be used in the synthesis of [(HgCl2)2(HgCl2)(2-bppt)]n where 2-bppt= bis[4-(pyridine-2-yl)pyrimidin-2-ylthio]methane.
It assists in the following reactions:
It may be used as a catalyst for the addition reaction between aromatic amines and terminal acetylenes. It may also be used in the synthesis of [(HgCl2)2(HgCl2)(2-bppt)]n where 2-bppt= bis[4-(pyridine-2-yl)pyrimidin-2-ylthio]methane.
It assists in the following reactions:
- Cyclization of amidinothioureas with phenyl hydrazine to afford 3-amino-1,2,4-triazole derivatives.
- Cyclization-rearrangement of O-propargyl glycolaldehyde dithioacetals leading to the formation of 3-pyranones.
- Reductive dimerization and cyclization of α,β-unsaturated ketones to generate 3,4-trans-diarylcyclopentanols.
품질
May contain black specks
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - Repr. 2 - Skin Corr. 1B - STOT RE 1
Storage Class Code
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
Mercury(II)chloride-mediated cyclization-Rearrangement of O-propargylglycolaldehyde dithioacetals to 3-pyranone dithioketals: An expeditious access to 3-pyranones.
Ghorai S and Bhattacharjya A.
Organic Letters, 7(2), 207-210 (2005)
Catalytic and non-catalytic addition of aromatic amines to terminal acetylenes in the presence of mercury (II) chloride and acetate.
Barluenga J, et al.
Journal of the Chemical Society. Perkin Transactions 1, 1980, 2732-2737 null
A one-dimensional coordination chain constructed by mercury (II) chloride and bis [4-(pyridine-2-yl) pyrimidin-2-ylthio] methane.
Zhu HB, et al.
J. Chem. Res. (M), 36(10), 598-599 (2012)
Electron diffraction investigation of gaseous mercury (II) chloride.
Kashiwabara K, et al.
Bulletin of the Chemical Society of Japan, 46(2), 410-413 (1973)
Zinc mediated reductive dimerization and cyclization of α β-unsaturated ketones in the presence of a catalytic amount of mercury (II) chloride.
Kapoor KK, et al.
Tetrahedron Letters, 46(37), 6253-6255 (2005)
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