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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Copper, bis(diethylcarbamodithioato-kS,kS')-, (SP-4-1)-

CCN(C(=S)[S-])CC.CCN(C(=S)[S-])CC.[Cu+2] Request for Quotation
Chemical Name: Copper, bis(diethylcarbamodithioato-kS,kS')-, (SP-4-1)-
CAS Number: 13681-87-3
Product Number: AG003PHX(AGN-PC-0PL3FY)
Synonyms:
MDL No:
Molecular Formula: C10H20CuN2S4
Molecular Weight: 360.0852

Identification/Properties

Properties
MP:
197°C
BP:
357.68°C (estimate)
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
360.07g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
358.981g/mol
Monoisotopic Mass:
358.981g/mol
Topological Polar Surface Area:
72.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
73
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Copper(II) diethyldithiocarbamate, often abbreviated as Cu(DDTC)2, is a versatile compound widely utilized in chemical synthesis. This coordination complex plays a crucial role in various chemical reactions due to its unique properties. In chemical synthesis, Copper(II) diethyldithiocarbamate acts as a catalyst or reagent in a range of reactions. Its ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it particularly valuable in organic synthesis. By serving as a catalyst, this compound enables the efficient and selective synthesis of complex organic molecules.Furthermore, Copper(II) diethyldithiocarbamate is often employed in the preparation of metal sulfides as well as in the development of coordination polymers. Its coordination chemistry also makes it a useful tool in the synthesis of coordination compounds for various applications.Overall, the application of Copper(II) diethyldithiocarbamate in chemical synthesis showcases its significance in enabling the creation of diverse chemical compounds through its catalytic and reactivity properties.