
CAS 70448-03-2: 1-Propanol, 2-(phenylmethoxy)-
Formula:C10H14O2
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Found 5 products.
2-(Benzyloxy)-1-propanol
CAS:Controlled ProductApplications 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 19940126Formula:C10H14O2Color and Shape:NeatMolecular weight:166.222-(Benzyloxy)-1-propanol-d6
CAS:Controlled ProductApplications 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);Formula:C21D3H29O11Color and Shape:NeatMolecular weight:463.4912-(Benzyloxy)propan-1-ol
CAS:Formula:C10H14O2Purity:97%Color and Shape:LiquidMolecular weight:166.2172-(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.Formula:C10H14O2Purity:Min. 95%Molecular weight:166.22 g/mol