Reference of 308087-58-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.308087-58-3, Name is 1-(4-Methylenepiperidin-1-yl)ethanone, molecular formula is C8H13NO. In a article，once mentioned of 308087-58-3
The p-type organic semiconductor (OSC) material tetrathieno[2,3-a:3?,2?-c:2?,3?-f:3?,2?-h]naphthalene (2TTN) and its alkyl-substituted derivatives Cn-2TTNs (n = 6, 8, and 10) have been developed based on the results of theoretical calculation-inspired investigation. A hole mobility for amorphous Cn-2TTNs (10-2-10-3 cm2 V-1 s-1) was accurately predicted by using a novel statistical method in which the geometric mean of the mobilities for many individual small molecular flocks in an amorphous solid was obtained by using molecular mechanical molecular dynamics simulations and quantum chemical calculations. The simulation also suggests that upon increasing the length of alkyl chains in Cn-2TTNs the mobilities become smaller as a consequence of a decrease in transfer integral values. Cn-2TTNs are synthesized in a microflow reactor through photoreactions of the corresponding precursors. Cn-2TTNs are then utilized in the fabrication of organic field-effect transistors (OFETs). Although spin-coated thin films of Cn-2TTNs are crystalline, the hole mobilities (10-2-10-3 cm2 V-1 s-1) of trial OFETs decrease upon elongation of the alkyl chains. This finding parallels the results of theoretical simulation. The simulation method for amorphous solids developed in this effort should become a useful tool in studies aimed at designing new OSC materials.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 308087-58-3, and how the biochemistry of the body works.Reference of 308087-58-3
Reference：
Piperidine – Wikipedia,
Piperidine | C5H6412N – PubChem