产品名称
Nickel(II) chloride, anhydrous for synthesis
SMILES string
[Ni+2].[Cl-].[Cl-]
InChI
1S/2ClH.Ni/h2*1H;/q;;+2/p-2
InChI key
QMMRZOWCJAIUJA-UHFFFAOYSA-L
grade
synthesis grade
vapor pressure
1.33 hPa ( 671 °C)
form
powder
potency
105 mg/kg LD50, oral (Rat)
pH
4 (20 °C, 500 g/L in H2O)
mp
1009 °C
density
3.55 g/cm3
storage temp.
2-30°C
Quality Level
Analysis Note
Assay (complexometric): 98.0 - 102.0 %
Loss on drying (150 °C; 3h): ≤ 1.0 %
Loss on drying (150 °C; 3h): ≤ 1.0 %
Application
Nickel(II) chloride can be used as a catalyst:
- To synthesize acyclic and cyclic dithioacetals via thioacetalization of aldehydes.
- To prepare α-aminonitrile derivatives via a one-pot, three-component coupling reaction of aldehydes, amines, and trimethylsilyl cyanide.
- In the hydrodefluorination of fluoroarenes in the presence of lithium triethylborohydride.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1A Inhalation - Muta. 2 - Repr. 1B - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1 Inhalation
target_organs
Lungs
存储类别
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
法规信息
危险化学品
此项目有
Highly Efficient Nickel (II) Chloride/Bis (tricyclohexylphosphine) nickel (II) Chloride-Cocatalyzed Hydrodefluorination of Fluoroarenes and Trifluorotoluenes with Superhydride
Zhao Wenwen, et al.
Advanced Synthesis & Catalysis, 354(4), 574-578 (2012)
Nickel (II) chloride as an efficient and useful catalyst for chemoselective thioacetalization of aldehydes
Khan AT, et al.
Tetrahedron Letters, 44(5), 919-922 (2003)
Highly Efficient Nickel (II) Chloride/Bis (tricyclohexylphosphine) nickel (II) Chloride-Cocatalyzed Hydrodefluorination of Fluoroarenes and Trifluorotoluenes with Superhydride
Zhao Wenwen, et al.
advanced synthesis and catalysis, 354(4), 574-578 (2012)
Nickel (II) chloride catalyzed one-pot synthesis of α-aminonitriles
De Surya Kanta
J. Mol. Catal. A: Chem., 225(2), 169-171 (2005)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持

