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Catalog | ACM69098153 |
CAS | 69098-15-3 |
Structure | ![]() |
Category | Flocculant |
Synonyms | Nickel(II) chloride |
IUPAC Name | Dichloronickel;hydrate |
Molecular Weight | 147.61 |
Molecular Formula | Cl2H2NiO |
Canonical SMILES | O.Cl[Ni]Cl |
InChI | InChI=1S/2ClH.Ni.H₂O/h2*1H;1H2/q;+2;/p-2 |
InChI Key | HGGYAQHDNDUIIQ-UHFFFAOYSA-L |
Melting Point | 1001 °C |
Purity | 99%+ |
Solubility | Freely soluble in water |
Appearance | Green crystalline aggregates |
Application | Nickel(II) Chloride Hydrate serves as a versatile catalyst in various chemical processes, particularly in electroplating and organic reactions. It plays a significant role in the chemo-selective thioacetalization of aldehydes and, when combined with lithium aluminum hydride, functions as an efficient reducing agent for alkenes, alkynes, and organic halides, while also effectively cleaving N-O bonds and opening epoxides. Furthermore, this compound acts as a precursor in forming nickel-phosphine complexes, such as bis(triphenylphosphine)nickel(II) chloride, which are pivotal in facilitating reactions like alkyne trimerizations, carbonylations, and Suzuki-Miyaura cross-coupling, offering an alternative to palladium-based catalysts. Additionally, it is integral to the synthesis of the acetylacetonate complex of nickel, which is essential for producing the 1,5-cyclooctadiene complex used in organonickel chemistry. Nickel(II) Chloride Hydrate can also be utilized in forming the sandwich compound nickelocene through its dimethoxyethane complex, thereby further enhancing its applications in catalysis. |
EC Number | 231-743-0 |
MDL Number | MFCD00149808 |
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