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Copper(I) Hexafluoroacetylacetonate 1,5-cyclooctadiene Complex

CAS #: 86233-74-1
Linear Formula:
(CF3COCHCOCF3)Cu(C8H12)
MDL Number
MFCD00156517
EC No.:
N/A

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Copper(I) Hexafluoroacetylacetonate 1,5-cyclooctadiene Complex CU-FACA15C-01-P SDS > Data Sheet >
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Copper(I) Hexafluoroacetylacetonate 1,5-cyclooctadiene Complex Properties (Theoretical)

Compound Formula C13H13CuF6O2
Molecular Weight 378.78
Appearance Yellow powder
Melting Point 93-100 °C
Boiling Point 60°C/0.1mm subl.
Density N/A
Solubility in H2O Insoluble
Exact Mass 378.012 g/mol
Monoisotopic Mass 378.012 g/mol

Copper(I) Hexafluoroacetylacetonate 1,5-cyclooctadiene Complex Health & Safety Information

Signal Word Warning
Hazard Statements H315-H319-H335
Hazard Codes Xi
Precautionary Statements P280g-P305+P351+P338
Risk Codes R36/37/38
Safety Statements N/A
Transport Information NONH for all modes of transport
GHS Pictogram
Image
Exclamation Point - GHS07

About Copper(I) Hexafluoroacetylacetonate 1,5-cyclooctadiene Complex

Copper(I) Hexafluoroacetylacetonate 1,5-cyclooctadiene Complex is an organometallic copper compound used as a precursor material for MOCVD applications. High purity, submicron and nanopowder forms may be considered. American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia) and follows applicable ASTM testing standards. Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available.

Synonyms

Copper(I) hexafluoro-2,4-pentanedionate 1,5-cyclooctadiene complex, copper(I) hexafluoroacetylacetonate complex with 1,5-cyclooctadiene, copper hexafluoroacetylacetonate cyclooctadiene, 1,5-Cyclooctadiene(hexafluoro-2,4-pentanedionato)copper(I)

Chemical Identifiers

Linear Formula (CF3COCHCOCF3)Cu(C8H12)
Pubchem CID 92043567
MDL Number MFCD00156517
EC No. N/A
IUPAC Name copper; cyclooctane; (Z)-1,1,1,5,5,5-hexafluoro-4-hydroxypent-3-en-2-one
Beilstein/Reaxys No.
SMILES C1C[CH][CH]CC[CH][CH]1.C(=C(C(F)(F)F)O)C(=O)C(F)(F)F.[Cu]
InchI Identifier InChI=1S/C8H12.C5H2F6O2.Cu/c1-2-4-6-8-7-5-3-1;6-4(7,8)2(12)1-3(13)5(9,10)11;/h1-2,7-8H,3-6H2;1,12H;/b;2-1-;
InchI Key WSAPIYREFIKPSH-FJOGWHKWSA-N
Chemical Formula
Molecular Weight
Standard InchI
Appearance
Melting Point
Boiling Point
Density

Packaging Specifications

Typical bulk packaging includes palletized plastic 5 gallon/25 kg. pails, fiber and steel drums to 1 ton super sacks in full container (FCL) or truck load (T/L) quantities. Research and sample quantities and hygroscopic, oxidizing or other air sensitive materials may be packaged under argon or vacuum. Shipping documentation includes a Certificate of Analysis and Safety Data Sheet (SDS). Solutions are packaged in polypropylene, plastic or glass jars up to palletized 440 gallon liquid totes, and 36,000 lb. tanker trucks.

Related Elements

See more Copper products. Copper Bohr Model Copper (atomic symbol: Cu, atomic number: 29) is a Block D, Group 11, Period 4 element with an atomic weight of 63.546. The number of electrons in each of copper's shells is 2, 8, 18, 1 and its electron configuration is [Ar]3d10 4s1. The copper atom has a radius of 128 pm and a Van der Waals radius of 186 pm. Copper was first discovered by Early Man prior to 9000 BC. In its elemental form, copper has a reddish-orange metallic and lustrous appearance. Of all pure metals, only silver Elemental Copperhas a higher electrical conductivity. The origin of the word copper comes from the Latin word 'cuprium' which translates as "metal of Cyprus," as the Mediterranean island of Cyprus was known as an ancient source of mined copper.

Fluorine is a Block P, Group 17, Period 2 element. Its electron configuration is [He]2s22p5. The fluorine atom has a covalent radius of 64 pm and its Van der Waals radius is 135 pm. In its elemental form, CAS 7782-41-4, fluorine gas has a pale yellow appearance. Fluorine was discovered by André-Marie Ampère in 1810. It was first isolated by Henri Moissan in 1886.