Brief introduction of 134419-59-3

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.Application In Synthesis of Tetrahydro-2H-pyran-4-yl methanesulfonate, you can also check out more blogs about134419-59-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.134419-59-3, Name is Tetrahydro-2H-pyran-4-yl methanesulfonate, molecular formula is C6H12O4S. In a Patent£¬once mentioned of 134419-59-3, Application In Synthesis of Tetrahydro-2H-pyran-4-yl methanesulfonate

DERIVATIVES OF PYRAZOLOPHENYL-BENZENESULFONAMDE COMPOUNDS AND USE THEREOF AS ANTITUMOR AGENTS

Substituted pyrazolophenyl-benzenesulfonamide compounds of formula (I) are described, wherein m, R1, R2, R3, and R4 are defined in the description, which modulate the activity of protein kinases, These compounds find utility in treating diseases caused by deregulated protein kinase activity, such as cancer and cell proliferative disorders

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.Application In Synthesis of Tetrahydro-2H-pyran-4-yl methanesulfonate, you can also check out more blogs about134419-59-3

Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics