CAS 65094-22-6
:bromodifluoromethane diethyl phosphate
Description:
Bromodifluoromethane diethyl phosphate, with the CAS number 65094-22-6, is a chemical compound that belongs to the class of organophosphates. It typically exhibits characteristics associated with both halogenated compounds and phosphate esters. The presence of bromine and fluorine atoms suggests that it may have significant volatility and potential reactivity, particularly in the presence of moisture or other nucleophiles. As a diethyl phosphate, it likely possesses two ethyl groups attached to the phosphate moiety, which can influence its solubility and polarity. This compound may be used in various applications, including as a flame retardant or in chemical synthesis. However, due to the presence of halogens, it may also raise environmental and health concerns, necessitating careful handling and disposal. Its specific physical and chemical properties, such as boiling point, melting point, and reactivity, would need to be referenced from detailed chemical databases or safety data sheets for precise information.
Formula:C5H10BrF2O3P
InChI:InChI=1/C5H10BrF2O3P/c1-3-10-12(9,11-4-2)5(6,7)8/h3-4H2,1-2H3
SMILES:CCOP(=O)(C(Br)(F)F)OCC
Synonyms:- Diethyl (bromodifluoromethyl)phosphonate
- Bromodifluoromethyl diethyl phosphonate
- Diethyl bromodifluoromethanephosphonate
- Bromodifluoromethyl diethylphosphonate
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Found 8 products.
Diethyl (Bromodifluoromethyl)phosphonate
CAS:Formula:C5H10BrF2O3PPurity:>97.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:267.01Diethyl (bromodifluoromethyl)phosphonate, 97%
CAS:<p>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</p>Formula:C5H10BrF2O3PPurity:97%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:267.01Bromodifluoromethyl diethylphosphonate
CAS:Formula:C5H10BrF2O3PPurity:95%Color and Shape:Liquid, ClearMolecular weight:267.007Diethyl Bromodifluoromethanephosphonate
CAS:Formula:C5H10BrF2O3PPurity:95%Color and Shape:LiquidMolecular weight:267.0057Diethyl (bromodifluoromethyl)phosphonate
CAS:Formula:C5H10BrF2O3PPurity:≥ 97.0%Color and Shape:Colourless to light yellow liquidMolecular weight:267.01Diethyl [bromo(difluoro)methyl]phosphonate
CAS:<p>Diethyl [bromo(difluoro)methyl]phosphonate</p>Formula:C5H10BrF2O3PPurity:97%Color and Shape: colourless liquidMolecular weight:267.00566g/molDiethyl Bromodifluoromethylphosphonate
CAS:Controlled Product<p>Applications 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.<br>References Zafrani, Y., et al.: Tetrahedron, 65, 5278 (2009); Talukdar, A., et al.: Bioorg. Med. Chem., 18, 3518 (2010)<br></p>Formula:C5H10BrF2O3PColor and Shape:NeatMolecular weight:267.01Diethyl (bromodifluoromethyl)phosphonate
CAS:<p>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.</p>Formula:C5H10BrF2O3PPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:267.01 g/mol







