Archives for Chemistry Experiments of Ethyl 3-oxopentanoate

Reference of 4949-44-4, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 4949-44-4.

Reference of 4949-44-4, As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 4949-44-4, Name is Ethyl 3-oxopentanoate, SMILES is CCC(CC(OCC)=O)=O, belongs to pyridazines compound. In a article, author is Lu Qiang, introduce new discover of the category.

Synthesis and Bioactivity of 1-Methyl-3-aryl-6(trifluoromethyl)pyridazin-4(1H)-one Derivatives

A novel series of 3-aryl pyridazinone was proposed on the base of structure activity relationships of diverse protoporphyrinogen oxidase inhibitors. Synthetic method of 3-aryl pyridazinones was investigated and 9 compounds were synthesized for interior screening test of herbicidal activity and crop safety. Bioassay results showed that most of 3-aryl-pyridazinones exhibit excellent pre-orpost-emergence herbicidal activity. Herein, 3-(2,4-dichloro-5-(cyclopentyloxy) phenyl)1-methyl-6-(trifluoromethyl) pyridazin-4(1H)-one(Ie) with high activity was selected as a post-herbicide candidate into corn field trial. The results showed that Ie exhibited higher total effective rate against weeds at the dose of 60 g a. i./hm(2) than mesotrione at 105 g a. i./hm(2), and safety to corn after emergence as well.

Reference of 4949-44-4, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 4949-44-4.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem