Properties and Exciting Facts About 2133-34-8

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.Safety of (S)-Azetidine-2-carboxylic acid, you can also check out more blogs about2133-34-8

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2133-34-8, Name is (S)-Azetidine-2-carboxylic acid, molecular formula is C4H7NO2. In a Patent£¬once mentioned of 2133-34-8, Safety of (S)-Azetidine-2-carboxylic acid

TRIAZOLO-1,4-DIAZEPINE DERIVATIVES AND THEIR USE IN PHARMACEUTICALS

A triazolo-1,4-di-azepine compound of the below given formulas and a pharmacologically acceptable salt thereof are disclosed and useful in the pharmaceutical field, especially to allergic diseases. STR1 in which R1 and R2 are hydrogen or an alkyl, R3 is hydrogen or a halogen, R4 is hydrogen or an alkyl, X is–OCO–,–NHCO–,–CO–or others and Y is a cycloalkyl, a cycloalkylalkyl, an alkynyl or others.

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.Safety of (S)-Azetidine-2-carboxylic acid, you can also check out more blogs about2133-34-8

Reference£º
Chiral Catalysts,
Chiral catalysts – SlideShare