CAS 70448-03-2
:1-Propanol, 2-(phénylméthoxy)-
2-(Benzyloxy)propan-1-ol
CAS :Formule :C10H14O2Degré de pureté :95%Couleur et forme :LiquidMasse moléculaire :166.21702-(Benzyloxy)-1-propanol-d6
CAS :Produit contrôléApplications 2-(Benzyloxy)-1-propanol-d6 is an intermediate in the synthesis of Isotope labelled Propylene Glycol 2-Glucuronide which is a metabolite of propylene glycol, used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds.
References Szczepankiewicz, B. et al.: J. Med. Chem., 49, 3563 (2006); Mateus, R. et al.: Int. J. Pharm., 444, 106 (2013);Formule :C21D3H29O11Couleur et forme :NeatMasse moléculaire :463.4912-(Benzyloxy)-1-propanol
CAS :Produit contrôléApplications 2-(Benzyloxy)-1-propanol is used to prepare amino diol HIV-protease inhibitors. It is also used to synthesize diphenyl-substituted amino alcohols as protease inhibitors.
References Chen, P., et al.: J. Med. Chem., 39, 1991 (1996); Gordon, E., et al.: Eur. Pat. Appl. (1994), EP 580402 A2 19940126Formule :C10H14O2Couleur et forme :NeatMasse moléculaire :166.222-(Benzyloxy)-1-propanol
CAS :2-(Benzyloxy)-1-propanol (2-BP) is a glycidol derivative that can be used to produce propanol. 2-BP reacts with Tenofovir, an antiviral drug, in the presence of enolate and organometallic catalysts to form acetaldehyde. 2-BP also reacts with chloride to form alkoxides, which are useful in the synthesis of adenine derivatives. In addition, 2-BP has been shown to react with vinyl ethers and alcohols in the presence of catalysis to form benzyl derivatives.
Formule :C10H14O2Degré de pureté :Min. 95%Masse moléculaire :166.22 g/molRef: 3D-VCA44803
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