New explortion of 1-Chloro-10H-phenothiazine

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 1910-85-6, you can also check out more blogs aboutProduct Details of 1910-85-6

Chemistry can be defined as the study of matter and the changes it undergoes. Product Details of 1910-85-6. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.1910-85-6, Name is 1-Chloro-10H-phenothiazine, molecular formula is C12H8ClNS, introducing its new discovery.

Studies on Diamagnetic Susceptibility of Biologically Active Heterocycles. 1. Diamagnetic Susceptibility of Phenothiazines

Diamagnetic susceptibilities for a number of phenothiazines are reported.A theoretical method to estimate the diamagnetic susceptibility of these biologically active heterocycles is presented.Phenothiazines have been considered to be composed of two units: one consisting of a benzene nucleus containing amino and thio groups at ortho positions to the substituents and the other consisting of a benzene ring with substituents.The diamagnetic contributions of these two units have been obtained from the diamagnetic susceptibilities of substituted o-aminobenzenethiols and benzenes and have been used in estimating the diamagnetic susceptibilities of phenothiazines.It has provided excellent theoretical results.Such an excellent agreement between measured and estimated values is due to the fact that the interactions between substituents which affect the diamagnetism have been duly accounted for in such calculations.

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 1910-85-6, you can also check out more blogs aboutProduct Details of 1910-85-6

Reference£º
Thiazine – an overview | ScienceDirect Topics,
Thiazine | C4H5NS – PubChem