The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.499-40-1, Name is (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal, molecular formula is C12H22O11. In a Article，once mentioned of 499-40-1, Product Details of 499-40-1
The iron(II) spin crossover dinuclear compound [Fe(dpa)(NCS)2] 2bpym where dpa = 2,2?-dipyridylamine and bpym = 2,2?-bipyrimidine has been synthesized and characterized. Variable-temperature magnetic susceptibility and 57Fe Moessbauer spectroscopy data provide evidence for a rather complete and continuous S=2 (HS)?S=0 (LS) spin-crossover behavior taking place in the temperature range 400-50 K (T1/2=245 K) without the presence of a plateau at 50% of conversion. The absence of such plateau, which is characteristic of all dinuclear compounds so far studied, is interpreted in terms of synergetic effect between intramolecular and intermolecular interactions.
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.Product Details of 499-40-1, you can also check out more blogs about499-40-1
Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics