685038
Tetrakisacetonitrile copper(I) triflate
Synonym(s):
Tetrakisacetonitrile copper(I) trifluoromethanesulfonate
About This Item
Recommended Products
form
solid
reaction suitability
core: copper
reagent type: catalyst
SMILES string
[Cu+].CC#N.CC#N.CC#N.CC#N.[O-]S(=O)(=O)C(F)(F)F
InChI
1S/4C2H3N.CHF3O3S.Cu/c4*1-2-3;2-1(3,4)8(5,6)7;/h4*1H3;(H,5,6,7);/q;;;;;+1/p-1
InChI key
NOBZSXGFNYRDMS-UHFFFAOYSA-M
Related Categories
Application
Copper(I)/ABNO-Catalyzed Aerobic Alcohol Oxidation: Alleviating Steric and Electronic Constraints of Cu/TEMPO Catalyst Systems
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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.
Customers Also Viewed
Articles
Alcohol oxidation yields aldehydes and ketones, crucial intermediates in organic synthesis.
Alcohol oxidation yields aldehydes and ketones, crucial intermediates in organic synthesis.
Alcohol oxidation yields aldehydes and ketones, crucial intermediates in organic synthesis.
Alcohol oxidation yields aldehydes and ketones, crucial intermediates in organic synthesis.
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