10256-92-5 Usage
Uses
Used in Organic Synthesis:
Urea, N,N,N',N'-tetrafluorois used as a solvent for organic synthesis, facilitating various chemical reactions due to its ability to dissolve a wide range of organic compounds.
Used in Fluorous Polymer Preparation:
In the field of polymer chemistry, Urea, N,N,N',N'-tetrafluorois utilized in the preparation of fluorous polymers, which have unique properties and potential applications in materials science.
Used as a Phase Transfer Catalyst:
Urea, N,N,N',N'-tetrafluoroserves as a phase transfer catalyst, enhancing the efficiency of reactions involving the transfer of reactants between immiscible phases, such as between an aqueous and an organic phase.
Used as a Fluorine Source in Organic Chemistry Reactions:
Due to its perfluorinated nature, Urea, N,N,N',N'-tetrafluorois used as a fluorine source in organic chemistry reactions, providing a convenient and effective means to introduce fluorine atoms into organic molecules.
Used in Medical Imaging:
Urea, N,N,N',N'-tetrafluorohas potential applications in medical imaging, where its ability to solubilize hydrophobic compounds can improve the contrast and resolution of imaging techniques.
Used in Drug Delivery:
In the pharmaceutical industry, Urea, N,N,N',N'-tetrafluorois used to enhance the bioavailability of hydrophobic drugs, improving their solubility and absorption in the body, thereby increasing their therapeutic efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 10256-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10256-92:
(7*1)+(6*0)+(5*2)+(4*5)+(3*6)+(2*9)+(1*2)=75
75 % 10 = 5
So 10256-92-5 is a valid CAS Registry Number.
10256-92-5Relevant academic research and scientific papers
Some chemistry of difluoraminocarbonyl fluoride, NF2CFO. The preparation of perfluorourea, (NF2)2CO, and difluoraminocarbonyl chloride, NF2C(O)Cl. New preparations for NF2OCF3 and NF2<
Fraser, George W.,Shreeve, Jean'ne M.
, p. 1711 - 1715 (2008/10/08)
Reactions of NF2CFO with CF3OF or with Al2Cl6 and HCl yield NF2OCF3 or NF2C(O)Cl, respectively. The reactions of NF2CFO with KF and CsF to give KOCF2NF
