930857
Ni(bpy)Cl2
Synonym(s):
[Bipyridine]nickel(II) dichloride
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C10H8Cl2N2Ni
CAS Number:
Molecular Weight:
285.78
MDL number:
UNSPSC Code:
12352103
NACRES:
NA.21
Recommended Products
![[4,4′-Bis(1,1-dimethylethyl)-2,2′-bipyridine] nickel (II) dichloride](/deepweb/assets/sigmaaldrich/product/structures/471/091/6faa29b1-bf8a-4d87-90b2-4cc55e082620/640/6faa29b1-bf8a-4d87-90b2-4cc55e082620.png)
![(Ir[dF(CF3)ppy]2(dtbpy))PF6](/deepweb/assets/sigmaaldrich/product/structures/982/913/02dd8ddd-6deb-40a0-ab9b-07b18f1abb09/640/02dd8ddd-6deb-40a0-ab9b-07b18f1abb09.png)
![[4,4′-Dimethyl-2,2′-bipyridine]nickel(II) dichloride hydrate ≥95%](/deepweb/assets/sigmaaldrich/product/structures/714/807/6f838a65-cb7b-400f-bdb3-3e207bb2ddc4/640/6f838a65-cb7b-400f-bdb3-3e207bb2ddc4.png)
![[Ni(dtbbpy)(H2O)4]Cl2](/deepweb/assets/sigmaaldrich/product/structures/777/629/15c13300-e874-4abd-8bd4-8b2bb4864570/640/15c13300-e874-4abd-8bd4-8b2bb4864570.png)
form
powder
Quality Level
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
greener alternative category
storage temp.
−20°C
SMILES string
Cl[Ni]1([N]2=CC=CC=C2C3=CC=CC=[N]31)Cl
Related Categories
General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Application
Ni(bpy)Cl2 is a nickel catalyst used for a variety of cross-coupling reactions.
related product
Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Sorry, we don't have COAs for this product available online at this time.
If you need assistance, please contact Customer Support.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of α-Aryl Secondary Amides via Nickel-Catalyzed Reductive Coupling of Redox-Active Esters.
Alexis L Gabbey et al.
Organic letters, 24(17), 3173-3178 (2022-04-27)
The transition-metal-catalyzed α-arylation of secondary amides remains a synthetic challenge due to the presence of a free N-H bond. We report a strategy to synthesize secondary α-aryl amides via a Ni-catalyzed reductive arylation of redox-active N-hydroxyphthalimide (NHP) esters of malonic
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