408366-18-7 Usage
Uses
Used in Pharmaceutical Industry:
4'-Trifluoromethoxy-biphenyl-2-carboxylic acid is used as a key intermediate in the synthesis of various drugs and medications. Its unique chemical structure allows for the development of new therapeutic agents with potential applications in the treatment of various diseases and disorders.
Used in Research and Development:
In the research industry, 4'-Trifluoromethoxy-biphenyl-2-carboxylic acid is utilized for studying its potential applications in drug development. Its reactivity and versatile properties make it a promising candidate for the creation of novel compounds with therapeutic potential.
Used in Material Science:
4'-Trifluoromethoxy-biphenyl-2-carboxylic acid is also researched for its potential use in material science. Its unique properties and reactivity contribute to the development of new materials with specific characteristics, further expanding its applications beyond the pharmaceutical realm.
Used in Organic Synthesis:
Due to its versatile properties, 4'-Trifluoromethoxy-biphenyl-2-carboxylic acid is employed in organic synthesis for the creation of various organic compounds. Its reactivity allows for the formation of new chemical entities with potential applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 408366-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,3,6 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 408366-18:
(8*4)+(7*0)+(6*8)+(5*3)+(4*6)+(3*6)+(2*1)+(1*8)=147
147 % 10 = 7
So 408366-18-7 is a valid CAS Registry Number.
408366-18-7Relevant academic research and scientific papers
General and practical carboxyl-group-directed remote C-H oxygenation reactions of arenes
Wang, Yang,Gulevich, Anton V.,Gevorgyan, Vladimir
, p. 15836 - 15840 (2014/04/03)
Two methods for remote aromatic C-H oxygenation reactions, have been developed. Method1, the Cu-catalyzed oxygenation reaction, is highly efficient for cyclization of electron-neutral and electron-rich biaryl carboxylic acids into 3,4-benzocoumarins. Method2, the K2S2O 8-mediated oxygenation reaction, is more general and practical for cyclization of substrates with electron-donating and -withdrawing groups (see scheme). Copyright
N-BENZODIOXOLYL, N-BENZODIOXANYL AND N-BENZODIOXEPINYL ARYLCARBONXAMIDE DERIVATIVES, AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM
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Page 44-45, (2010/02/06)
The present invention relates to a compound of the formula (I) : in which T, A, R, B Xi, Yi and n are as defined in Claim 1, and to the pharmaceutically usable derivatives, solvates and stereoisomers thereof, comprising a mixture thereof in all proportions, which can be used in the treatment of dyslipidaemia, and to pharmaceutical compositions comprising them.
