Fluanisone

2-Amino-4-fluorophenol

Biochem/physiol Actions The metabolism and excretion of the xenobiotic compound 2-fluoroaniline is important due to human exposure in manufacturing. It is found to be very efficiently metabolized, primarily by 4-hydroxylation with subsequent

Biochem/physiol Actions The metabolism and excretion of the xenobiotic compound 2-fluoroaniline is important due to human exposure in manufacturing. It is found to be very efficiently metabolized, primarily by 4-hydroxylation with subsequent

Application 2-Fluorophenyl isothiocyanate has been used in the synthesis of acylthiosemicarbazides .

Application Reactant for: Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation Site-selective

Application Reactant for: Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation Site-selective

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 3-Fluoro-2-methylaniline was used in the synthesis of 2-amino-1,7,9-trimethylimidazo[4,5- g ]quinoxaline .

Application Recently used to make novel liquid crystalline fluorobiphenylcyclohexenes and difluoroterphenyls by palladium-catalyzed cross-couplings also used in the synthesis of o -phenylphenols as potent leukotriene B4 receptor agonists. Other

Application Recently used to make novel liquid crystalline fluorobiphenylcyclohexenes and difluoroterphenyls by palladium-catalyzed cross-couplings also used in the synthesis of o -phenylphenols as potent leukotriene B4 receptor agonists. Other

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 4-Fluoro-2-methylaniline was used in the synthesis of 4-fluoro- N -[( E )-{7-methoxy-2-[4-(methylsulfanyl)phenyl]-1-benzofuran-5-yl}methylidene]-2-methylaniline .