Some scientific research about cis-Cyclohexane-1,2-diamine

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of: cis-Cyclohexane-1,2-diamine, you can also check out more blogs about1436-59-5

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1436-59-5, Name is cis-Cyclohexane-1,2-diamine, molecular formula is C6H14N2. In a Article,once mentioned of 1436-59-5, Quality Control of: cis-Cyclohexane-1,2-diamine

4-(E)-2-[3-(3-[(E)-2-(4-Cyanophenyl)-1-diazenyl]perhydrobenzo[d] imidazol-1-ylmethyl) perhydrobenzo[d]imidazol-1-yl]-1-diazenylbenzonitrile (1) has been synthesized by reaction of p-cyanobenzene diazonium chloride with a mixture of formaldehyde and trans-1,2-cyclohexanediamine. The crystal structure has been determined by single crystal X-ray diffraction analysis. The bis-triazene (1) does not adopt a folded conformation, unlike previously studied ethylenediamine analogues, and there is no indication of pi-stacking in the crystal packing. The dominant interaction between molecules is the van der Waal’s attraction between cyclohexane rings. This result establishes the structure of the product of this diazonium coupling reaction as the 1-(1-imidazolidinylmethyl)imidazolidine derivative and not the alternate tetraazabicyclo[4.4.1]undecane derivative. Crystal data: 1 C29H 34N10, orthorhombic, space group Pbca, a = 17.946(1), 6 = 13.106(1), c = 24.108(1) A, V = 5670.6(3) A3, for Z = 8.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of: cis-Cyclohexane-1,2-diamine, you can also check out more blogs about1436-59-5

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare