Chemical Research Letters, April 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 21834-92-4, Name is 5-Methyl-2-phenylhex-2-enal, molecular formula is C13H16O, Product Details of 21834-92-4, belongs to isothiazole compound, is a common compound. In a patnet, author is Cutri, CCC, once mentioned the new application about 21834-92-4.
A series of 4-isothiazolecarbonitriles was synthesized and screened for in vitro antiviral activity. The effect of various substituents on the phenyl ring, as well as the substitution of the phenyl for other aromatic and heteroaromatic rings, was examined to establish the requirements for optimum activity. The most active member of the series, 3-methylthio-5-phenyl-4-isothiazolecarbonitrile, exhibited a high level of activity against enteroviruses polio 1 and ECHO 9. Preliminary studies on its mechanism of action indicated that this compound had an effect on an early event in the replication of poliovirus type 1. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield. If you are hungry for even more, make sure to check my other article about 21834-92-4, Product Details of 21834-92-4.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com