CAS 30310-22-6
:2-Bromo-4-méthylpentane
- 4-Methyl-2-pentyl bromide
- Pentane, 2-bromo-4-methyl-
- 2-Bromo-4-methylpentane
Pentane, 2-bromo-4-methyl-
CAS :Formule :C6H13BrDegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :165.07142-Bromo-4-methylpentane
CAS :Formule :C6H13BrDegré de pureté :95%Couleur et forme :Liquid, OilMasse moléculaire :165.0742-Bromo-4-methylpentane
CAS :Produit contrôléApplications 2-Bromo-4-methylpentane is an alkyl bromide and a substituent in the synthesis of various pharmaceutical goods.
References Epstein, W. W., et al.: J. Chem. Soc., 20, 1338 (1970); Tokura, N., et al.: Bull. Chem. Soc., Jap., 33, 1176 (1960); Do, H. Q., et al.: J. Am. Chem. Soc., 136, 2162 (2014);Formule :C6H13BrCouleur et forme :NeatMasse moléculaire :165.0712-Bromo-4-methylpentane
CAS :2-Bromo-4-methylpentane is an isomeric, branched-chain fatty acid. It has been observed to desorb from the surface of polyethylene terephthalate in a conformational fashion. This reaction was shown to be first order with respect to bromine concentration and was found to be reversible. The kinetics were found to be second order with respect to bromine concentration and first order with respect to polyethylene terephthalate surface area. The rates of the desorption of 2-bromo-4-methylpentane were found not to be affected by the presence of chloride ions.
2-Bromo-4-methylpentane can also undergo a Suzuki coupling reaction with amines in the presence of palladium catalysts and chiral phosphoric acid ligands. This reaction can produce substituted benzo[b]thiophenes, which are useful for organic synthesis reactions such as phthalFormule :C6H13BrDegré de pureté :Min. 95%Masse moléculaire :165.08 g/mol





