CAS 65094-22-6
:Bromdifluormethan Diethylphosphat
- Diethyl (bromodifluoromethyl)phosphonate
- Bromodifluoromethyl diethyl phosphonate
- Diethyl bromodifluoromethanephosphonate
- Bromodifluoromethyl diethylphosphonate
Diethyl (Bromodifluoromethyl)phosphonate
CAS:Formel:C5H10BrF2O3PReinheit:>97.0%(GC)Farbe und Form:Colorless to Almost colorless clear liquidMolekulargewicht:267.01Diethyl (bromodifluoromethyl)phosphonate, 97%
CAS:Diethyl (bromodifluoromethyl)phosphonate is used as a reactant for the preparation of phosphopeptide mimetic prodrugs targeted to Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 (Stat3), synthesis of Mycobacterium tuberculosis protein tyrosine phosphatase inhibitory
Formel:C5H10BrF2O3PReinheit:97%Farbe und Form:Clear colorless to pale yellow, LiquidMolekulargewicht:267.01Bromodifluoromethyl diethylphosphonate
CAS:Formel:C5H10BrF2O3PReinheit:95%Farbe und Form:Liquid, ClearMolekulargewicht:267.007Diethyl Bromodifluoromethanephosphonate
CAS:Formel:C5H10BrF2O3PReinheit:95%Farbe und Form:LiquidMolekulargewicht:267.0057Diethyl (bromodifluoromethyl)phosphonate
CAS:Formel:C5H10BrF2O3PReinheit:≥ 97.0%Farbe und Form:Colourless to light yellow liquidMolekulargewicht:267.01Diethyl [bromo(difluoro)methyl]phosphonate
CAS:Diethyl [bromo(difluoro)methyl]phosphonateFormel:C5H10BrF2O3PReinheit:97%Farbe und Form: colourless liquidMolekulargewicht:267.00566g/molDiethyl Bromodifluoromethylphosphonate
CAS:Kontrolliertes ProduktApplications Diethyl Bromodifluoromethylphosphonate is a highly efficient and environmentally benign difluorocarbene precursor. It can be used as a reagent in the synthesis of benzindolone structural scaffolds for inhibition of lumazine synthase.
References Zafrani, Y., et al.: Tetrahedron, 65, 5278 (2009); Talukdar, A., et al.: Bioorg. Med. Chem., 18, 3518 (2010)Formel:C5H10BrF2O3PFarbe und Form:NeatMolekulargewicht:267.01Diethyl (bromodifluoromethyl)phosphonate
CAS:Diethyl (bromodifluoromethyl)phosphonate is a functional group that can be used in nucleophilic reactions. It is an electrophile and a strong nucleophile. Diethyl (bromodifluoromethyl)phosphonate reacts with amines to form phosphonamides and with boronic acids to form phosphine oxides. Diethyl (bromodifluoromethyl)phosphonate has been used in preparative chemistry to cleave bonds, such as the bond between the two ethylene glycol units in diethylene glycol methyl ether. Diethyl (bromodifluoromethyl)phosphonate also increases bone resorption through its interaction with calcium ions, which are essential for maintaining bone health.
Formel:C5H10BrF2O3PReinheit:Min. 95%Farbe und Form:Colorless Clear LiquidMolekulargewicht:267.01 g/mol







