
CAS 503070-57-3
:2-(2-(6-bromohexyloxy)éthoxyméthyl)-1,3-dichlorobenzène
Benzene, 2-[[2-[(6-Bromohexyl)Oxy]ethOxy]Methyl]-1,3-Dichloro
CAS :Formule :C15H21BrCl2O2Degré de pureté :97%Couleur et forme :LiquidMasse moléculaire :384.1360Vilanterol Impurity 28
CAS :Formule :C15H21BrCl2O2Couleur et forme :Pale Yellow LiquidMasse moléculaire :384.142-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS :2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzeneDegré de pureté :98%Masse moléculaire :384.14g/mol2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS :Produit contrôléApplications 2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene is an intermediate in the synthesis of Vilanterol Trifenatate-d4 (V260002). Vilanterol Trifenatate (V260000) is a long-acting β2 adrenergic receptor Agonist. It demonstrates prolonged bronchodilation in subjects with asthma and COPD.
References Procopiou, P., et al.: J. Med. Chem., 53, 4522 (2010); Kempsford, R., et al.: Pulm. Pharmacol. Ther., 26,Formule :C15H21BrCl2O2Couleur et forme :NeatMasse moléculaire :384.142-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene-d4
CAS :Produit contrôléApplications 2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene-d4 is the isotope labelled analog of 2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene which is an intermediate in the synthesis of Vilanterol Trifenatate-d4 (V260002). Vilanterol Trifenatate (V260000) is a long-acting β2 adrenergic receptor Agonist. It demonstrates prolonged bronchodilation in subjects with asthma and COPD.
References Procopiou, P., et al.: J. Med. Chem., 53, 4522 (2010); Kempsford, R., et al.: Pulm. Pharmacol. Ther., 26,Formule :C15H17D4BrCl2O2Couleur et forme :NeatMasse moléculaire :388.162-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS :Formule :C15H21BrCl2O2Degré de pureté :97%Couleur et forme :SolidMasse moléculaire :384.142-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS :2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene is an organic compound that belongs to the family of carbamic acid derivatives. It has a primary amino group and a carbamic acid at the 2 and 3 positions, respectively. This molecule also has a formyl group on the 1 position. The amination reaction between this compound and formaldehyde will produce an imine as a final product. This reaction is catalyzed by heat or other oxidants like nitric acid or hydrogen peroxide. The formylation of this molecule is used in industrial preparations for the synthesis of chiral compounds with high selectivity for one enantiomer over another. The synthetic process can be carried out with high yield and the reaction selectivity is not affected by other factors such as pH or temperature changes.
Formule :C15H21BrCl2O2Degré de pureté :Min. 95%Masse moléculaire :384.14 g/mol






