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(E)-1-(4-ethylphenyl)-2-[4-(4-trans-n-propylcyclohexyl)phenyl]ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

207614-41-3

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207614-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207614-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,1 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 207614-41:
(8*2)+(7*0)+(6*7)+(5*6)+(4*1)+(3*4)+(2*4)+(1*1)=113
113 % 10 = 3
So 207614-41-3 is a valid CAS Registry Number.

207614-41-3Downstream Products

207614-41-3Relevant academic research and scientific papers

Stereodivergent ruthenium-catalyzed transfer semihydrogenation of diaryl alkynes

Li, Jie,Hua, Ruimao

, p. 8462 - 8465 (2011)

[Ru3(CO)12]-catalyzed transfer semihydrogenation of various functionalized diaryl alkynes with N,N-dimethylformamide (DMF) and water as hydrogen source affords cis- and trans-stilbenes. The stereodivergent approach can be switched by the use of acetic (HOAc) or trifluoroacetic (TFA) acid as additives. The catalytic processes can be applied to the synthesis of analogues of natural products such as cis-combretastatin A-4 and trans-resveratrol. Copyright

Nickel-Catalyzed Stereodivergent Synthesis of E- and Z-Alkenes by Hydrogenation of Alkynes

Murugesan, Kathiravan,Bheeter, Charles Beromeo,Linnebank, Pim R.,Spannenberg, Anke,Reek, Joost N. H.,Jagadeesh, Rajenahally V.,Beller, Matthias

, p. 3363 - 3369 (2019/06/28)

A convenient protocol for stereodivergent hydrogenation of alkynes to E- and Z-alkenes by using nickel catalysts was developed. Simple Ni(NO3)2?6 H2O as a catalyst precursor formed active nanoparticles, which were effective for the semihydrogenation of several alkynes with high selectivity for the Z-alkene (Z/E>99:1). Upon addition of specific multidentate ligands (triphos, tetraphos), the resulting molecular catalysts were highly selective for the E-alkene products (E/Z>99:1). Mechanistic studies revealed that the Z-alkene-selective catalyst was heterogeneous whereas the E-alkene-selective catalyst was homogeneous. In the latter case, the alkyne was first hydrogenated to a Z-alkene, which was subsequently isomerized to the E-alkene. This proposal was supported by density functional theory calculations. This synthetic methodology was shown to be generally applicable in >40 examples and scalable to multigram-scale experiments.

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