Details
| Stereochemistry | RACEMIC |
| Molecular Formula | 2C8H15O2.Cu |
| Molecular Weight | 349.953 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cu++].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O
InChI
InChIKey=SEKCXMNFUDONGJ-UHFFFAOYSA-L
InChI=1S/2C8H16O2.Cu/c2*1-3-5-6-7(4-2)8(9)10;/h2*7H,3-6H2,1-2H3,(H,9,10);/q;;+2/p-2
DescriptionSources: DOI: 10.1002/047084289X.rn01567Curator's Comment: description was created based on several sources, including:
https://fscimage.fishersci.com/msds/98967.htm
Sources: DOI: 10.1002/047084289X.rn01567
Curator's Comment: description was created based on several sources, including:
https://fscimage.fishersci.com/msds/98967.htm
CUPRIC BIS(2-ETHYLHEXANOATE) has been used as is used as a Lewis acid, as an oxidant, as a catalyst/promoter of alkene amination reactions, and as an organic soluble copper(II) carboxylate in reaction kinetics. The powder is an irritant to the eyes, respiratory system, and skin. Avoid contact with skin and eyes, and avoid dust inhalation.
Approval Year
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SUBSTANCE RECORD