Synthetic Route of 1111-67-7, Some examples of the diverse research done by chemistry experts include discovery of new medicines and vaccines, improving understanding of environmental issues, and development of new chemical products and materials. In an article,authors is Pettinari, Claudio, once mentioned the application of Synthetic Route of 1111-67-7, Name is Cuprous thiocyanate, is a conventional compound.
Several new complexes of the type [Cu(NO3)(PPh3)2(L)m] (L=3-methylpyrazole, 4-methylpyrazole, 3,5-dimethylpyrazole, 4-bromopyrazole or bis(4-methylpyrazol-1-yl)methane, m=1; L=pyrazole, 1,2,4-triazole or 2-methylimidazole, m=2), [Cu(NO3)(PPh3)(L)] (L=3,4,5-trimethylpyrazole or 4-phenylimidazole), [Cu(NO)3(PAr3)n(L)3] (Ar=p- or m-tolyl, n=0 or 1, L=pyrazole),[CuX(PPh3)2(L)] (X=Cl, Br or I, L=pyrazole or 3,5-dimethylpyrazole) and [CuX(PPh3)(L)] (X=Cl or Br, L=bis(pyrazol-1-yl)methane, bis(3,5-dimethy lpyrazol-1-yl)methane or bis(triazol-1-yl)methane) have been prepared and characterized by analytical and spectral data. The compounds [CuX(PPh3)(L)] (X=Cl, Br or I, L=pyrazole or 3,5-dimethylpyrazole) are fluxional at temperature above 240 K. The dinuclear compound [Cu2(PPh3)3(pzH)2] was obtained when the reaction between [CuI(PPh3)3] and pyrazole (pzH) wascarried out in methanol containing alkali. In the crystal structure of the title compound, the copper atom is found in a strongly distorted tet rahedral coordination [P-Cu-P: 128.0(1)°] with two long Cu-O distances [2.217(9) and 2.184(9) A].
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Synthetic Route of 1111-67-7, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Synthetic Route of 1111-67-7
Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”