2268-15-7 Usage
Description
2,3,5-Trifluorophenol is an organic compound with the chemical formula C6H3F3OH. It is characterized by the presence of three fluorine atoms at the 2nd, 3rd, and 5th positions of a phenol molecule. 2,3,5-TRIFLUOROPHENOL is a clear light yellow liquid after melting and is known for its unique chemical properties.
Uses
Used in the Chemical Industry:
2,3,5-Trifluorophenol is used as a building block for the synthesis of various polyurethane derivatives. Its presence in the molecular structure enhances the properties of the resulting materials, such as their durability, flexibility, and resistance to degradation.
Used in the Plastics Industry:
2,3,5-Trifluorophenol is used as a monomer in the production of polyurethane plastics. These plastics are known for their versatility and are used in a wide range of applications, including automotive components, insulation materials, and consumer goods.
Used in the Pharmaceutical Industry:
2,3,5-Trifluorophenol is also utilized as an intermediate in the synthesis of certain pharmaceutical compounds. Its unique chemical properties make it a valuable component in the development of new drugs and medications.
Used in the Coatings Industry:
2,3,5-Trifluorophenol is employed in the formulation of coatings, such as paints and varnishes, due to its ability to improve the durability and resistance of the final product. Its incorporation into coatings can lead to enhanced performance and longer-lasting protection for various surfaces.
Check Digit Verification of cas no
The CAS Registry Mumber 2268-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2268-15:
(6*2)+(5*2)+(4*6)+(3*8)+(2*1)+(1*5)=77
77 % 10 = 7
So 2268-15-7 is a valid CAS Registry Number.
2268-15-7Relevant articles and documents
Homolytic Reactions of Polyfluoroaromatic Compounds. Part 16. Competitive Phenylation of Polyfluorobenzenes
Allen, Kim J.,Bolton, Roger,Williams, Gareth H.
, p. 691 - 696 (2007/10/02)
Pairs of polyfluorobenzenes were allowed to compete for phenyl radicals generated by thermolysis of benzoyl peroxide at 80 deg C.From the relative yields of biaryl, and the yields of each biaryl formed upon arylation of each arene individually, the relative rates of attack of each site in each arene were deduced.Neither iron(III) benzoate nor trichloroacetic acid uniformly improved yields of biaryl, although in some cases the isomer distribution altered, when decomposition of benzoyl peroxide was carried out in the presence of such additives, to favour products of aryldehydrogenation or of aryldefluorination, respectively.Competition did not usually affect the distribution of attack of a particular arene, except when hexafluorobenzene was used, in which case greater selectivity of attack of the second arene occured.This suggested the formation of a 'stabilised' phenyl radical, and supported an earlier suggestion of species such as >; other evidence also supported the postulate.
