Product Details of 86-29-3. In 2019 J ORG CHEM published article about BISPHOSPHONATE INHIBITION; MECHANISM; SYNTHASE; DESIGN in [Kaboudin, Babak; Esfandiari, Hesam; Moradi, Atieh; Kazemi, Foad] IASBS, Dept Chem, Gava Zang 4513766731, Zanjan, Iran; [Aoyama, Hiroshi] Tokyo Univ Pharm & Life Sci, Sch Pharm, 1432-1 Horinouchi, Hachioji, Tokyo 1920392, Japan in 2019, Cited 41. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3.
In this study, the double addition of dialkylphosphite to nitriles in a ZnCl2/Et3N system is described. The reaction was conveniently and directly used for the synthesis of biologically important 1-aminobisphosphonates (ABPs) from nitriles. The one-pot synthesis of 1-aminobisphosphonates from aldehydes via the in situ generation of nitriles is also described.
Product Details of 86-29-3. About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Kaboudin, B; Esfandiari, H; Moradi, A; Kazemi, F; Aoyama, H or concate me.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem