406206-10-8 Usage
Molecular structure
Contains a benzene ring with a hydroxyphenyl group and a trifluoromethyl group attached to it, and a nitrile functional group (C≡N) at the 6th position of the benzene ring.
Usage
Commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals.
Application
Utilized in organic synthesis as a versatile intermediate in the production of a wide range of chemical products.
Importance in research
Its trifluoromethyl group makes it a valuable compound for research and development in the field of medicinal chemistry and drug discovery due to the unique properties it can impart to potential drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 406206-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,2,0 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 406206-10:
(8*4)+(7*0)+(6*6)+(5*2)+(4*0)+(3*6)+(2*1)+(1*0)=98
98 % 10 = 8
So 406206-10-8 is a valid CAS Registry Number.
406206-10-8Relevant articles and documents
Synthesis of phloroglucinol monoaryl ethers
Sherwood, Alexander M.,Pond, David M.,Trudell, Mark L.
scheme or table, p. 1208 - 1212 (2012/05/20)
A variety of novel functionalized phloroglucinol monoaryl ethers have been synthesized using a two-step procedure. Target ethers were synthesized by coupling electron-deficient aryl fluorides with 3,5-dimethoxyphenol via nucleophilic aromatic substitution (SNAr) in N-methylpyrrolidone and cesium carbonate. Subsequent boron tribromide-mediated demethylation gave a series of phloroglucinol monoaryl ethers in good overall yields. Georg Thieme Verlag Stuttgart New York.
