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Copper(II) 2-ethylhexanoate

ALDRICH/337323

Synonym: 2-Ethylhexanoic acid copper(2+) salt; Copper bis(2-ethylhexanoate); Copper di(2-ethylhexanoate); Copper(2+) 2-ethylhexanoate; Cupric bis(2-ethylhexanoate)

CAS Number: 149-11-1
Empirical Formula (Hill Notation): C16H30CuO4
Molecular Weight: 349.95
EC Number: 205-731-0
MDL Number: MFCD00015695
Linear Formula: [CH3(CH2)3CH(C2H5)CO2]2Cu
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-337323-5G 5 g
 $51.50
1/EA		 Add To Favorites
45-337323-25G 25 g
 $185.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 337323-25G

 

composition Cu, 17.0-19.0% EDTA titration
form powder or chunks
  solid
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
InChI key SEKCXMNFUDONGJ-UHFFFAOYSA-L
mp 252 °C (dec.) (lit.)
Quality Level 100 
reaction suitability core: copper
  reagent type: catalyst
SMILES string CCCCC(CC)C(=O)O[Cu]OC(=O)C(CC)CCCC
Application:
  • Copper catalyzed Heck-like cyclizations of oxime esters: Discusses the catalytic role of Copper(II) 2-ethylhexanoate in cyclization reactions and its potential reduction or disproportionation under certain conditions (Faulkner et al., 2014 ).
  • A Copper‐Mediated Oxidative Coupling Route to 3H‐ and 1H‐Indoles: Utilizes Copper(II) 2-ethylhexanoate for synthesizing indoles, showcasing its effectiveness in facilitating novel chemical transformations (Drouhin & Taylor, 2015 ).
  • Cu (II) carboxylate arene C─H functionalization: Details how Copper(II) 2-ethylhexanoate is used in nonradical pathways for functionalizing aromatic compounds, significantly advancing synthetic chemistry methodologies (Kong et al., 2022 ).
  • Decarboxylative olefination of activated aliphatic acids: Describes the catalytic capabilities of Copper(II) 2-ethylhexanoate in decarboxylative olefination processes, enhancing the efficiency and scope of organic syntheses (Tlahuext-Aca et al., 2018 ).
Packaging: 5, 25 g in glass bottle
mp 252 °C (dec.) (lit.)
UNSPSC 12352300

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