In 2021.0 RSC ADV published article about ONE-POT SYNTHESIS; FE3O4 NANOPARTICLES; REUSABLE CATALYST; HIGHLY EFFICIENT; BIFUNCTIONAL NANOCATALYST; MULTICOMPONENT SYNTHESIS; HETEROGENEOUS CATALYST; SAPONINS; NANOCOMPOSITE; ALKALOIDS in [Kazemnejadi, Milad; Nasseri, Mohammad Ali; Sheikh, Safoora; Rezazadeh, Zinat; Gol, Seyyedeh Ameneh Alavi] Univ Birjand, Fac Sci, Dept Chem, POB 97175-615, Birjand, Iran; [Sheikh, Safoora] Univ Regensburg, Inst Organ Chem, Univ Str 31, D-93053 Regensburg, Germany in 2021.0, Cited 76.0. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7. Formula: C9H10O3
Saponin, as a green and available phytochemical, was immobilized on the surface of magnetite nanoparticles then doped with Cu ions (Fe3O4@Sap/Cu(ii)) and used as an efficient nanocatalyst for the synthesis of quinazoline and acridine derivatives, due to their high application and importance in various fields of science. Different spectroscopic and microscopic techniques were used for the catalyst characterization such as FT-IR, XRD, FE-SEM, EDX, TEM, TGA, VSM, BET, DLS, CV, and XPS analyses. All characterization data were correlated with each other so that the structure of the catalyst was accurately characterized. The reactions were performed in the presence of a low amount of Fe3O4@Sap/Cu(ii) (0.42 mol%) as a green catalyst in water over a short period of time. The results show well the effective role of saponin in solving the problem of mass transfer in aqueous medium, which is the challenge of many organic reactions in aqueous medium and in the presence of heterogeneous medium. High catalytic activity was found for the catalyst and high to excellent efficiency was obtained for all quinazoline (68-94% yield) and acridine (66-97% yield) derivatives in short reaction times (less than 1 hour) under mild reaction conditions in the absence of any hazardous or expensive materials. There is not any noticeable by-product found whether for acridine or quinazoline derivatives, which reflects the high selectivity. Two reasonable mechanisms were proposed for the reactions based on observations from control experiments as well as literature reports. The catalyst could be easily recovered magnetically for at least six consecutive runs with insignificant reactivity loss.
Formula: C9H10O3. Welcome to talk about 93-02-7, If you have any questions, you can contact Kazemnejadi, M; Nasseri, MA; Sheikh, S; Rezazadeh, Z; Gol, SAA or send Email.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com