One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of 3,4-Dichloro-1H-pyrrole-2,5-dione, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 1193-54-0, Name is 3,4-Dichloro-1H-pyrrole-2,5-dione, molecular formula is C4HCl2NO2
Acylation of Amines with Dichloromaleoyl Chloride
The reaction of dichloromaleoyl chloride (2) with ammonia in ether yields the ammonium salt of (Z)-2,3-dichloro-3-cyanoacrylic acid (6) and with aqueous ammonia the ammonium salt of (Z)-2-amino-3-chloro-3-cyanoacrylic acid (1).With primary aliphatic and aromatic amines dichloromaleamides 8 are obtained, the two chlorine atoms of which can be replaced with other amines to form after cis/trans isomerization diaminofumaramides 11.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Safety of 3,4-Dichloro-1H-pyrrole-2,5-dione, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 1193-54-0
Reference£º
Pyrroline – Wikipedia,
1-Pyrroline | C4H7N – PubChem