6816-12-2 Usage
Uses
Used in Pharmaceutical Industry:
[(difluoroamino)oxy](fluoro)sulfane dioxide is used as an intermediate or reagent for the synthesis of various pharmaceutical compounds due to its unique combination of fluorine, nitrogen, oxygen, and sulfur atoms. This can be particularly useful in the development of new drugs with specific properties or improved efficacy.
Used in Organic Synthesis:
In the field of organic synthesis, [(difluoroamino)oxy](fluoro)sulfane dioxide can be utilized as a building block or a catalyst for creating complex organic molecules. Its fluorine and nitrogen content may facilitate reactions that are otherwise difficult to achieve, leading to the production of novel organic compounds.
Used in Agrochemicals:
[(difluoroamino)oxy](fluoro)sulfane dioxide may find applications in the agrochemical industry, potentially as a component in the development of new pesticides, herbicides, or fertilizers. [(difluoroamino)oxy](fluoro)sulfane dioxide's properties could contribute to the creation of more effective and environmentally friendly products for agricultural use.
Used in Chemical Research:
Due to its unique elemental composition, [(difluoroamino)oxy](fluoro)sulfane dioxide can be a valuable subject for research in organic chemistry and chemical engineering. It may be used in experiments to study reaction mechanisms, explore new synthetic pathways, or investigate the effects of fluorine and nitrogen in various chemical contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 6816-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6816-12:
(6*6)+(5*8)+(4*1)+(3*6)+(2*1)+(1*2)=102
102 % 10 = 2
So 6816-12-2 is a valid CAS Registry Number.
6816-12-2Relevant academic research and scientific papers
Some chemistry of difluoraminocarbonyl chloride. A new route to perfluorourea
Wright, Kenneth J.,Shreeve, Jean'ne M.
, p. 77 - 80 (2007/10/12)
Improved yields of NF2C(O)Cl are obtained by short-term (4-6 hr) photolysis of N2F4 with oxalyl chloride. Reactions of NF2C(O)Cl with AgCN, AgNCS, AgNCO, Hg(SCF3)2 and Hg(ON(CF3)2)2 give the new difluoraminocarbonyl pseudohalides NF2C(O)CN, NF2C(O)NCS, NF2C(O)NCO, NF2C(O)SCF3, and NF2C(O)ON(CF3)2. With excess of either Ag2O at 0° or HgO at -78°, NF2C(O)Cl is converted to (NF2)2CO and CO2 in nearly quantitative yield. Chlorocarbonyl fluorosulfate results when NF2C(O)Cl is mixed with S2O6F2 or BrOSO2F.
