What I Wish Everyone Knew About C2H4N4

Computed Properties of C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Sayed, GH; Azab, ME; Anwer, KE or send Email.

An article Conventional and Microwave-Assisted Synthesis and Biological Activity Study of Novel Heterocycles Containing Pyran Moiety WOS:000474012000001 published article about FACILE SYNTHESIS; DERIVATIVES; EFFICIENT in [Sayed, Galal H.; Azab, Mohammad E.; Anwer, Kuris E.] Ain Shams Univ, Organ Chem Lab, Chem Dept, Fac Sci, Cairo 11566, Egypt in 2019.0, Cited 30.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Computed Properties of C2H4N4

Under both conventional and microwave methods, 2-amino-4H-pyran-3-carbonitrile derivative 1 was synthesized and reacted with different reagents. Thus, 2-amino-4H-pyran-3-carbonitrile derivative was treated with chloroacetyl chloride, phenyl isocyanate, cyanoacetic acid, benzoyl chloride, triethyl orthoformate, acetic anhydride/H2SO4, arylidene malononitrile, urea, and/or p-aminosulphaguanidine producing chloroacetamide, 3-phenylurea, cyanoacetamide, N-benzoylpyran, ethylformimidate, pyranopyrimidin-4-one, pyranopyridine, pyranopyrimidin-2-one, and pyranopyrimidin-2-imine derivatives, respectively. Meanwhile, compound 1 was reacted with ethyl bromoacetate, phenacyl bromide, phthalic anhydride, different aromatic amines, and/or acetic acid/H2SO4 to produce 5-aminopyrano[2,3-b]pyrrole-6-carboxylate, dihydropyrano[2,3-b]pyrrole-6-yl-(phenyl)methanone, 1,3-dioxoisoindolinyl pyran, 1,4-dihydropyridine, and 2-hydroxy-1,4-dihydropyridine derivatives, respectively. On the other hand, when compound 1 was allowed to react with maleic anhydride and/or hydrazine hydrate, pyran-4-oxobut-2-enoic acid and 3-aminopyranopyrazole derivatives were obtained, respectively. Reaction of pyran-4-oxobut-2-enoic acid with malononitrile under different conditions gave 2-(furan-2-yl)-4H-pyran and 2-(4H-pyran-2-yl)-1H-pyrrole derivatives, while condensation of 3-aminopyranopyrazole with benzaldehyde gave 1,4-dihydropyrano[2,3-c]pyrazol-3-yl-1-phenylmethanimine derivative. The newly synthesized compounds were characterized by the spectroscopic tools IR, H-1-NMR, C-13-NMR, MS, and elemental analysis. Some of these compounds have been screened in vitro for antimicrobial activity against different strains of bacteria and fungi and also were tested against two cancer cell lines: mammary gland breast cancer (MCF-7) and colon cancer (HCT-118).

Computed Properties of C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Sayed, GH; Azab, ME; Anwer, KE or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics