54912-87-7 Usage
General Description
1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL is a chemical compound with a complex molecular structure. It is an organic compound that contains fluorine atoms, trifluoromethyl groups, and a diol functional group. 1,1,1,7,7,7-HEXAFLUORO-2,6-BIS(TRIFLUOROMETHYL)-3-HEPTENE-2,6-DIOL is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is known for its high thermal stability, chemical inertness, and unique reactivity, making it a valuable tool for organic synthesis. Additionally, its fluorinated nature also imparts unique physical and chemical properties, which makes it useful in various applications such as in the development of new materials and in the field of fluorine chemistry.
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 articles and documents
SYNTHESIS AND TRIMERIZATION OF FLUORINATED TERTIARY CYANATES
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.
