510475
Bis(methylcyclopentadienyl)nickel(II)
97%
Synonym(s):
1,1′-Dimethylnickelocene
About This Item
Recommended Products
Assay
97%
form
liquid
reaction suitability
core: nickel
reagent type: catalyst
bp
85-90 °C/1 mmHg (lit.)
mp
34-36 °C (lit.)
storage temp.
2-8°C
SMILES string
[Ni].C[C]1[CH][CH][CH][CH]1.C[C]2[CH][CH][CH][CH]2
InChI
1S/2C6H7.Ni/c2*1-6-4-2-3-5-6;/h2*2-5H,1H3;
InChI key
IHRNDXJDUYVDRB-UHFFFAOYSA-N
Related Categories
Application
- Nickel sandwich complexes
- N-heterocyclic carbene complexes
- Functionally substituted monocyclopentadienyl compounds
Features and Benefits
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service