
CAS 503070-57-3
:2-(2-(6-bromohexyloxy)ethoxymethyl)-1,3-dichlorobenzene
Description:
2-(2-(6-bromohexyloxy)ethoxymethyl)-1,3-dichlorobenzene is an organic compound characterized by its complex structure, which includes a dichlorobenzene core substituted with an ethoxymethyl group and a bromohexyloxy side chain. The presence of chlorine atoms on the benzene ring contributes to its reactivity and potential applications in various chemical processes. The bromohexyloxy group enhances the compound's hydrophobic properties, making it suitable for use in formulations requiring solubility in organic solvents. This compound may exhibit biological activity due to its halogenated structure, which can influence interactions with biological targets. Additionally, the presence of multiple functional groups suggests potential for further chemical modifications, making it a candidate for research in fields such as medicinal chemistry or materials science. Safety and handling precautions should be observed due to the presence of bromine and chlorine, which can pose health risks. Overall, this compound's unique structure and properties make it of interest in various chemical and industrial applications.
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 8 products.
Benzene, 2-[[2-[(6-Bromohexyl)Oxy]ethOxy]Methyl]-1,3-Dichloro
CAS:Formula:C15H21BrCl2O2Purity:97%Color and Shape:LiquidMolecular weight:384.13602-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS:2-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzenePurity:98%Molecular weight:384.14g/molVilanterol Impurity 28
CAS:Formula:C15H21BrCl2O2Color and Shape:Pale Yellow LiquidMolecular weight:384.142-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene-d4
CAS:Controlled Product<p>Applications 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.<br>References Procopiou, P., et al.: J. Med. Chem., 53, 4522 (2010); Kempsford, R., et al.: Pulm. Pharmacol. Ther., 26,<br></p>Formula:C15H17D4BrCl2O2Color and Shape:NeatMolecular weight:388.162-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS:Formula:C15H21BrCl2O2Purity:97%Color and Shape:SolidMolecular weight:384.142-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS:Controlled Product<p>Applications 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.<br>References Procopiou, P., et al.: J. Med. Chem., 53, 4522 (2010); Kempsford, R., et al.: Pulm. Pharmacol. Ther., 26,<br></p>Formula:C15H21BrCl2O2Color and Shape:NeatMolecular weight:384.142-[2-(6-Bromohexyloxy)ethoxymethyl]-1,3-dichlorobenzene
CAS:<p>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.</p>Formula:C15H21BrCl2O2Purity:Min. 95%Molecular weight:384.14 g/mol






