Final Thoughts on Chemistry for 37622-90-5

If you are interested in 37622-90-5, you can contact me at any time and look forward to more communication. Computed Properties of C6H8N2O2.

In an article, author is Metwally, Nadia Hanafy, once mentioned the application of 37622-90-5, Computed Properties of C6H8N2O2, Name is Ethyl 4-pyrazolecarboxylate, molecular formula is C6H8N2O2, molecular weight is 140.14, MDL number is MFCD00010844, category is pyrazoles-derivatives. Now introduce a scientific discovery about this category.

Synthesis, reactions, and antimicrobial activity of2-cyano-N ‘-(4-(2-oxo-2-phenylethoxy)benzylidene)acetohydrazide derivatives

Knovenagel condensation of the starting 2-cyano-N ‘-(4-(2-oxo-2-phenylethoxy)-benzylidene)acetohydrazide with different aromatic aldehydes produced the comparable arylidenes derivatives. Else way, 2-cyano-N ‘-(4-(2-oxo-2-phenylethoxy)-benzylidene)-acetohydrazide condensed witho-hydroxybenzaldehydes affording the respective chromenes which latter underwent acid hydrolysis giving the oxo-chromenes analogues. Moreover, the reaction of 2-cyano-N ‘-(4-(2-oxo-2-phenylethoxy)benzylidene)acetohydrazide with istain yielded the respective indeno[2,1-b]furan derivative that was converted to its oxo-analogue through acid hydrolysis. The treatment of 2-cyano-N ‘-(4-(2-oxo-2-phenylethoxy)benzylidene)acetohydrazide with alpha-halocompounds produced the relevant thiazoles. The enamine 2-cyano-3-(dimethylamino)-N ‘-(4-(2-oxo-2-phenylethoxy)benzylidene)acrylohydrazide underwent nucleophilic substitution reaction with guanidine hydrochloride followed by heterocyclization to get the relative aminopyrimidine. Contrarily, the reaction with various 4-arylazo-3,5-diaminopyrazoles provided the relative pyrazolo[1,5-a]pyrimidines. The antimicrobial investigation was carried out for some of the newly synthesized compounds using agar well diffusion method.

If you are interested in 37622-90-5, you can contact me at any time and look forward to more communication. Computed Properties of C6H8N2O2.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics