In 2019 BIOORG CHEM published article about INHIBITOR INHIBITORY-ACTIVITY; MUSHROOM TYROSINASE; ANTIVIRAL EVALUATION; ANTICANCER; ANTIBACTERIAL; ELUCIDATION; INSIGHTS in [Chortani, Sarra; Horchani, Mabrouk; Ben Jannet, Hichem; Romdhane, Anis] Univ Monasrir, Fac Sci Monastir, Lab Heterocycl Chem Nat Prod & React LR11ES39, Team Med Chem & Nat Prod, Ave Environm, Monastir 5019, Tunisia; [Nimbarte, Vijaykumar D.] Univ Havre, UFR Sci & Tech, Lab Chem, URCOM,EA 3221,INC3M CNRS,F3038, BP 1123,25 Rue Philipe Lebon, F-76063 Le Havre, France in 2019, Cited 44. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Product Details of 88-68-6
2-substitued-benzopyrimidinones 2 were synthesized in high to excellent yields in a single step via condensation of 2-aminobenzamide 1 with some aryl-aldehydes in the presence of iodine. Cyclocondensation reaction of hydrazides 3 which were obtained in two steps from benzopyrimidinones 2, with some electrophilic species such as 2,4-pentandione, 2,5-hexandione, 1-phenylbutan-1,3-dione and cyclic anyhdrides provided the new compounds 4a-c, 5a-c, 6a-c, 7a-c, 8a-c and 9a-c. The synthesized compounds were characterized by spectroscopic means. They were also evaluated for their anti-tyrosinase potential. The structure-activity relationship (SAR) was discussed on the basis of the molecular docking analysis.
Product Details of 88-68-6. Welcome to talk about 88-68-6, If you have any questions, you can contact Chortani, S; Nimbarte, VD; Horchani, M; Ben Jannet, H; Romdhane, A or send Email.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem