445-83-0 Usage
Description
4-Fluoro-2-nitroanisole is a chemical compound formed during the photolysis of the charge transfer complex of tetranitromethane and 4-fluoroanisole in dichloromethane at -20°C. It is characterized by its yellow powder appearance.
Uses
Since the provided materials do not specify any particular uses for 4-Fluoro-2-nitroanisole, it is not possible to list its applications based on the given information. However, if there were any known uses, they would be described as follows:
Used in [Application Industry]:
4-Fluoro-2-nitroanisole is used as [application type] for [application reason]
For example, if it were used in the pharmaceutical industry, the description would be:
Used in Pharmaceutical Industry:
4-Fluoro-2-nitroanisole is used as an intermediate compound for the synthesis of various pharmaceutical products due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 445-83-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 445-83:
(5*4)+(4*4)+(3*5)+(2*8)+(1*3)=70
70 % 10 = 0
So 445-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6FNO3/c1-12-7-3-2-5(8)4-6(7)9(10)11/h2-4H,1H3
445-83-0Relevant articles and documents
MODULATORS OF ATP-BINDING CASSETTE TRANSPORTERS
-
Page/Page column 230-231, (2010/02/11)
-
13C NMR Spectra of Substituted o-Nitroanisoles and n-Butyl o-Nitrophenyl Ethers
Zeegers, Petrus J.,Thompson, Malcolm J.
, p. 497 - 499 (2007/10/02)
13C NMR analyses of substituted o-nitroanisoles and n-butyl o-nitrophenyl ethers are reported. Key Words: 13C NMR - o-Nitroanisoles - n-Butyl o-nitrophenyl ethers
REGIOSPECIFIC SYNTHESIS OF CERTAIN 1,2,3,4-TETRASUBSTITUTED BENZENES IN ONE STEP VIA A BENZENE CYCLIZATION
Fisher, Lawrence E.,Caroon, Joan M.
, p. 233 - 238 (2007/10/02)
Tetrasubstituted benzenes of type 3 are obtained regiospecifically in a single step by the treatment of 1-fluoro-4-methoxy-5-carbo-tert-butoxy aniline with tert-butyllithium followed by reaction with an elecrophile.