54912-87-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL is used as a building block for the synthesis of pharmaceuticals due to its unique reactivity and the properties imparted by its fluorinated structure, which can enhance the performance and efficacy of the resulting drugs.
Used in Agrochemical Development:
In the agrochemical industry, 1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL serves as a key intermediate in the creation of novel agrochemicals, leveraging its thermal stability and chemical inertness to improve the performance of these products in agricultural applications.
Used in Specialty Chemicals Production:
1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL is utilized as a crucial component in the production of specialty chemicals, where its unique properties contribute to the development of innovative and high-performance materials for various industrial applications.
Used in Material Development:
1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL is used in the development of new materials, capitalizing on its fluorinated nature to create materials with specialized properties that can be applied in a range of industries, from electronics to aerospace.
Used in Fluorine Chemistry Research:
1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL is employed in the field of fluorine chemistry, where its unique properties are explored for advancing the understanding and application of fluorinated compounds in chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 54912-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,1 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54912-87:
(7*5)+(6*4)+(5*9)+(4*1)+(3*2)+(2*8)+(1*7)=137
137 % 10 = 7
So 54912-87-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F12O2/c10-6(11,12)4(22,7(13,14)15)2-1-3-5(23,8(16,17)18)9(19,20)21/h1-2,22-23H,3H2/b2-1+
54912-87-7Relevant academic research and scientific papers
Snow, Arthur W.,Griffith, James R.
, p. 471 - 486 (1980)
Monofunctional and bifunctional bis(α,α-trifluoromethyl) cyanates were prepared by reaction of a fluorinated alkoxide with cyanogen bromide or cyanogen chloride.In the synthesis of bifunctional cyanates, the cyanation reaction required sufficient intramolecular separation for independent functional group reactivity.Monofunctional cyanates could be rapidly quantitatively trimerized to cyclic cyanurates by catalytic quantities of AlCl3.Polymerization by trimerization of bifunctional cyanates under identical conditions was not succesful, apparently, due to encasement of the catalyst by the polymer network.
