Can You Really Do Chemisty Experiments About 4-(Trifluoromethyl)benzoic acid

Interested yet? Read on for other articles about 455-24-3, you can contact me at any time and look forward to more communication. Application In Synthesis of 4-(Trifluoromethyl)benzoic acid.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 455-24-3, Name is 4-(Trifluoromethyl)benzoic acid, SMILES is C1=C(C=CC(=C1)C(O)=O)C(F)(F)F, in an article , author is Gao, Dan, once mentioned of 455-24-3, Application In Synthesis of 4-(Trifluoromethyl)benzoic acid.

Selective Synthesis in Microdroplets of 2-Phenyl-2,3-dihydrophthalazine-1,4-dione from Phenyl Hydrazine with Phthalic Anhydride or Phthalic Acid

Pyridazine derivatives are privileged structures because of their potential biological and optical properties. Traditional synthetic methods usually require acid or base as a catalyst under reflux conditions with reaction times ranging from hours to a few days or require microwave assistance to induce the reaction. Herein, this work presents the accelerated synthesis of a pyridazine derivative, 2-phenyl-2,3-dihydrophthalazine-1,4-dione (PDHP), in electrosprayed microdroplets containing an equimolar mixture of phenyl hydrazine and phthalic anhydride or phthalic acid. This reaction occurred on the submillisecond timescale with good yield (over 90 % with the choice of solvent) without using an external catalyst at room temperature. In sharp contrast to the bulk reaction of obtaining a mixture of two products, the reaction in confined microdroplets yields only the important six-membered heterocyclic product PDHP. Results indicated that surface reactions in microdroplets with low pH values cause selectivity, acceleration, and high yields.

Interested yet? Read on for other articles about 455-24-3, you can contact me at any time and look forward to more communication. Application In Synthesis of 4-(Trifluoromethyl)benzoic acid.

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