133573-37-2 Usage
Molecular weight
350.14 g/mol The total mass of the molecule, calculated by adding the atomic weights of all the atoms present.
Fluorine content
High The compound has a significant number of fluorine atoms, which may contribute to its unique properties and reactivity.
Oxygen content
Moderate The presence of multiple oxygen atoms may affect the compound's polarity and solubility.
Trifluoroethenyl group
A key structural feature This group is a vinyl radical with three fluorine atoms, which may influence the compound's chemical properties and reactivity.
Central propan-1-ol molecule
Core structure The central alcohol group serves as the backbone for the attachment of other functional groups and atoms.
Complex structure
Challenging to predict reactivity Due to the presence of multiple fluorine and oxygen atoms, as well as the trifluoroethenyl group, the compound's reactivity and behavior in chemical reactions may be difficult to predict.
Industrial and research applications
Potential uses The unique structure and properties of 2,2,3,3-tetrafluoro-3-({1,1,1,2,3,3-hexafluoro-3-[(trifluoroethenyl)oxy]propan-2-yl}oxy)propan-1-ol may make it valuable in various industrial and research settings, such as the development of new materials or chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 133573-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,7 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133573-37:
(8*1)+(7*3)+(6*3)+(5*5)+(4*7)+(3*3)+(2*3)+(1*7)=122
122 % 10 = 2
So 133573-37-2 is a valid CAS Registry Number.
133573-37-2Relevant academic research and scientific papers
Hung, Ming-H.,Farnham, William B.,Feiring, Andrew E.,Rozen, Shlomo
, p. 8954 - 8959 (1993)
Linear and cyclic perfluorinated polyethers are prepared by a new route involving polymerization of a trifluorovinyl ether alcohol (CF2=CFORfCH2OH (1), Rf = CF2CF(CF3)OCF2CF2) followed by fluorination of the intermediate polyfluorinated polyethers. Polymerization occurs by ionic addition of OH groups to trifluorovinyl ether groups. In the absence of solvent, linear polymers with Mn values up to 29000 are obtained in excellent yield. In glyme solution, cyclic oligomers are the major products and a cyclic dimer is obtained in yields as high as 60%. Fluorinated macrodiols with Mn values to 5000 are obtained by copolymerization of 1 with a fluorinated diol. The intermediate linear and cyclic partially fluorinated polyethers have excellent solubility in organic solvents and the cyclics can complex anions through hydrogen bonding. Photofluorination of these polyethers with elemental fluorine in perfluorinated solvents proceeds smoothly with little fragmentation to afford the corresponding perfluorinated analogues in excellent yield.
