Product Information
- (R)-(-)-2-(Benzyloxymethyl)oxirane
- (+)-(Benzyloxymethyl)oxirane
- (+)-Benzyl glycidyl ether
- (-)-(R)-1,2-Epoxy-3-(benzyloxy)propane
- (-)-2-(Benzyloxymethyl)oxirane
- (-)-Benzyl-(R)-Glycidylether
- (-)-Benzyl-(R)-glycidyl ether
- (-)-Glycidyl benzyl ether
- (2R)-2-(Phenylmethoxymethyl)oxirane
- (2R)-2-[(Phenylmethoxy)methyl]oxirane
- See more synonyms
- (2R)-2-[(benzyloxy)methyl]oxirane
- (2S)-2-[(benzyloxy)methyl]oxirane
- (R)-(-)-Benzylglycidol
- (R)-1-Benzyloxy-2,3-epoxypropane
- (R)-2-(Benzyloxymethyl)oxirane
- (R)-Benzyloxymethyl-Oxirane
- (R)-Benzyloxymethyloxirane
- (R)-Glycidol benzyl ether
- (R)-O-Benzylglycidol
- (S)-Benzyl glycidyl ether
- 2-[(Benzyloxy)methyl]oxirane
- Benzyl (R)-2-epoxypropyl ether
- Oxirane, 2-[(phenylmethoxy)methyl]-
- Oxirane, 2-[(phenylmethoxy)methyl]-, (2R)-
- Oxirane, [(phenylmethoxy)methyl]-
- Oxirane, [(phenylmethoxy)methyl]-, (2R)-
- Oxirane, [(phenylmethoxy)methyl]-, (R)-
- Propane, 1-(benzyloxy)-2,3-epoxy-, (R)-
(R)-(-)-Glycidyl benzyl ether is an epoxide that can be synthesized by the reaction of glycidol and benzyl chloride with a chiral catalyst. This compound has been shown to have good oral bioavailability in vivo, and it is also stereoselective. The synthesis of (R)-(-)-Glycidyl benzyl ether involves a four-step process with a yield of around 60%. The first step involves the synthesis of glycidol, which can be accomplished with the help of an organometallic reagent such as n-butyllithium. The second step involves the addition of benzyl chloride to glycidol to produce 1,2-epoxycyclohexane. The third step entails hydrogenation of 1,2-epoxycyclohexane to form (R)-(-)-Glycidyl benzyl ether in high yield. Finally, the fourth step is the removal of hydrogen chloride
Chemical properties
Technical inquiry about: 3D-FG30975 (R)-(-)-Glycidyl benzyl ether
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