Recommanded Product: 123-11-5. Authors Rao, TN; Krishnarao, N; Ahmed, F; Alomar, SY; Albalawi, F; Mani, P; Aljaafari, A; Parvatamma, B; Arshi, N; Kumar, S in MDPI published article about in [Rao, Tentu Nageswara; Krishnarao, Nalla] Krishna Univ, Dept Chem, Machilipatnam 521001, Andhra Pradesh, India; [Ahmed, Faheem; Aljaafari, Abdullah; Kumar, Shalendra] King Faisal Univ, Dept Phys, Coll Sci, Al Hufuf 31982, Al Ahsa, Saudi Arabia; [Alomar, Suliman Yousef] King Saud Univ, Zool Dept, Coll Sci, Doping Res Chair, Riyadh 11451, Saudi Arabia; [Albalawi, Fadwa] King Saud Univ, Zool Dept, Coll Sci, Riyadh 11451, Saudi Arabia; [Mani, Panagal] Dept Biotechnol, Annai Coll Arts Sci, Kumbakonam 612503, Tamil Nadu, India; [Parvatamma, Botsa] GayathriPG Courses, Dept Organ Chem, Gotlam, Vizianagaram 530045, India; [Arshi, Nishat] King Faisal Univ, Dept Basic Sci, Preparatory Year Deanship, Al Hufuf, Al Ahsa, Saudi Arabia; [Kumar, Shalendra] Univ Petr & Energy Studies, Sch Engn, Dept Phys, Dehra Dun 248007, Uttarakhand, India in 2021, Cited 37. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5
A simple and highly efficient protocol for the synthesis of derivatives 7, 7-dimethyl-4-phenyl-2-thioxo-2, 3, 4, 6, 7, 8-hexahydro-1H-quinazoline-5-one from 5, 5-dimethyl cyclohexane-1, 3-dione (4a-4h) (dimedone) has been described. The aryl aldehydes were substituted with thiourea in the presence of synthesized zinc ferrite nanocatalyst, which increased the yield under reflux through condensation, followed by cyclization to give desired products. The other advantages are that it is eco-friendly and economically affordable for large-scale production. Structural validation and characterization of all the newly synthesized compounds were evaluated by spectral analysis (mass spectrometry, proton nuclear magnetic resonance ((HNMR)-H-1), and Carbon-13 nuclear magnetic resonance((CNMR)-C-13)spectroscopies. The structure of antibacterial and antifungal assays was performed with the newly synthesized compounds. The antimicrobial activity of title compounds possessing electron-withdrawing groups such as (4e-4h) (Cl, Br, and cyano group) exhibited more active potential than the electron-donating groups, C6H5,4-C6H4, 3-OC2H5-4OH-C6H3, etc., (4a-4d) containing moiety.
Recommanded Product: 123-11-5. Bye, fridends, I hope you can learn more about C8H8O2, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles