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线性分子式:
HgCl2
化学文摘社编号:
分子量:
271.50
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-299-8
MDL number:
Assay:
≥99.5%
Grade:
ACS reagent
Form:
powder
Solubility:
acetic acid: soluble(lit.)
acetone: soluble in salt form(lit.)
alcohol: soluble(lit.)
diethyl ether: passes test
ethyl acetate: soluble(lit.)
glycerol: soluble(lit.)
water: soluble(lit.)
acetone: soluble in salt form(lit.)
alcohol: soluble(lit.)
diethyl ether: passes test
ethyl acetate: soluble(lit.)
glycerol: soluble(lit.)
water: soluble(lit.)
产品名称
氯化汞(II), ACS reagent, ≥99.5%
assay
≥99.5%
form
powder
vapor pressure
1.3 mmHg ( 236 °C)
InChI key
LWJROJCJINYWOX-UHFFFAOYSA-L
InChI
1S/2ClH.Hg/h2*1H;/q;;+2/p-2
SMILES string
Cl[Hg]Cl
grade
ACS reagent
reaction suitability
reagent type: catalyst
core: mercury
reduction residue
≤0.02%
mp
277 °C (lit.)
solubility
acetic acid: soluble(lit.)
acetone: soluble in salt form(lit.)
alcohol: soluble(lit.)
diethyl ether: passes test
ethyl acetate: soluble(lit.)
glycerol: soluble(lit.)
water: soluble(lit.)
cation traces
Fe: ≤0.002%
Quality Level
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Application
Mercury (II) chloride can be used as a catalyst for the:
- Addition reaction between aromatic amines to terminal acetylenes to give imines, enamines, and 1,2,3,4-tetrahydroquinoline derivatives.
- Cyclization of amidinothioureas with phenyl hydrazine to produce 3-amino-1,2,4-triazole derivatives.
- Cyclization of O-propargyl glycolaldehyde dithioacetals to afford 3-pyranones along with 2,5-dihydrofuran-3-carboxaldehydes through their dithioketals and dithioacetals reaction.
- Reductive dimerization and cyclization of α,β-unsaturated ketones produce functionalized cyclopentanols using N,N-dimethylformamide as solvent.
General description
Mercury (II) chloride is an inorganic salt commonly used as a catalyst in organic synthesis.
signalword
Danger
Hazard Classifications
Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - Repr. 2 - Skin Corr. 1B - STOT RE 1
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
监管及禁止进口产品
此项目有
Ashley E Peppriell et al.
Toxicology, 443, 152561-152561 (2020-08-18)
Methylmercury (MeHg) is a ubiquitous environmental contaminant and developmental toxicant known to cause a variety of persistent motor and cognitive deficits. While previous research has focused predominantly on neurotoxic MeHg effects, emerging evidence points to a myotoxic role whereby MeHg
Mercury(II) Chloride.
Koc ovsky P.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2001)
Eagleson M.
Concise Encyclopedia Chemistry, 498-498 (1994)
Vasco Branco et al.
Free radical biology & medicine, 52(4), 781-793 (2011-12-27)
Mercury compounds exert toxic effects via interaction with many vital enzymes involved in antioxidant regulation, such as selenoenzymes thioredoxin reductase (TrxR) and glutathione peroxidase (GPx). Selenium supplementation can reactivate the mercury-inhibited TrxR and recover the cell viability in vitro. To
Igor Shuryak et al.
Scientific reports, 9(1), 11361-11361 (2019-08-08)
Exposure to chronic ionizing radiation (CIR) from nuclear power plant accidents, acts of terrorism, and space exploration poses serious threats to humans. Fungi are a group of highly radiation-resistant eukaryotes, and an understanding of fungal CIR resistance mechanisms holds the
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