Encyclopedia

  • Collision induced dissociation of N-(pyridin-2-yl)-substituted benzo(thio)amides and N-(isoquinolin-1-yl)furan(thiophene)-2-carboxamides and their difluoroboranyl derivatives
  • Add time:07/15/2019         Source:sciencedirect.com

    The effect of the properties of sulfur and oxygen atoms and of the presence/absence of the BF2 group on the collision induced dissociation (CID) behavior of singly charged ions generated by electrospray ionization (ESI) of N-(pyridin-2-yl)-substituted benzo(thio)amides and N-(isoquinolin-1-yl)furan(thiophene)-2-carboxamides and their difluoroboranyl derivatives has been investigated. The results show that O/S replacement (both in the amide/thioamide and the furan/thiophene moieties) has a strong influence on the CID fragmentation patterns. The loss of HOBF2 (or HSBF2) has been observed in ESI-CID MS/MS experiments performed for all difluoroboranyl derivatives. It can serve as a signature tag for the presence of the OBF2 (SBF2) moiety.

    We also recommend Trading Suppliers and Manufacturers of 3-(pyridin-2-yl)isoquinolin-1-amine (cas 37989-04-1). Pls Click Website Link as below: cas 37989-04-1 suppliers


    Prev:Tetrazolylmethyl quinolines: Design, docking studies, synthesis, anticancer and antifungal analyses
    Next: Pharmacokinetic profile of 3β-hydroxy-17-(1H-1,2,3-triazol-1-yl)androsta-5,16-diene (VN/87-1), a potent androgen synthesis inhibitor, in mice)

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View