The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, and theoretical assessments of solvent structures and their interactions with reaction intermediates and transition states. 144690-92-6, Name is Triphenyl methyl olmesartan, SMILES is O=C(C1=C(C(C)(O)C)N=C(CCC)N1CC2=CC=C(C3=CC=CC=C3C4=NN=NN4C(C5=CC=CC=C5)(C6=CC=CC=C6)C7=CC=CC=C7)C=C2)OCC8=C(C)OC(O8)=O, in an article , author is Liu Lei-Fang, once mentioned of 144690-92-6, Related Products of 144690-92-6.
The title compound, C18H13N3O2, has been synthesized for the first time by the multicomponent reaction of cyclopentanone, malononitrile and benzo[d][1,3]dioxole-5-carbaldehyde in the presence of triethylamine. The structure has been determined by NMR, MS and single-crystal X-ray diffraction. The crystal belongs to the triclinic system, space group P (1) over bar with a = 10.476(5), b = 10.973(5), c = 13.825(5) angstrom, alpha = 87.244(5), beta = 73.296(5), gamma = 82.097(5)degrees, C18H13N3O2, M-r = 303.31, V = 1507.6(11) angstrom(3), Z = 4, D-c = 1.336 g/cm(3), F(000) = 632, mu = 0.090 mm(-1), R = 0.0431 and wR = 0.1051. There exist intermolecular N-H center dot center dot center dot N hydrogen bonds in the title compound.
Related Products of 144690-92-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 144690-92-6.
Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem