CAS 14618-80-5: Benzyl (-)-glycidyl ether
Formula:C10H12O2
InChI:InChI=1S/C10H12O2/c1-2-4-9(5-3-1)6-11-7-10-8-12-10/h1-5,10H,6-8H2/t10-/m0/s1
InChI key:InChIKey=QNYBOILAKBSWFG-JTQLQIEISA-N
SMILES:C(OCC1=CC=CC=C1)[C@H]2CO2
Synonyms:- (+)-(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
- (2R)-2-[(benzyloxy)methyl]oxirane
- (2S)-2-[(benzyloxy)methyl]oxirane
- See more synonyms
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Found 6 products.
(R)-2-((Benzyloxy)methyl)oxirane
CAS:Purity:98.0%Color and Shape:Liquid, ClearMolecular weight:164.20399475097656Benzyl (R)-(-)-glycidyl ether, 98+%
CAS:Benzyl (R)-(-)-glycidyl ether is used in the preparation of the lactone fragment of compactin and mevinolin. Chiron in the preparation of syn-1,3-polyols, dideoxynucleosides, and a spiroacetal cyanohydrin. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C10H12O2Purity:98+%Color and Shape:Clear colorless, LiquidMolecular weight:164.20(R)-(-)-Glycidyl benzyl ether
CAS:(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 chlorideFormula:C10H12O2Purity:Min. 95%Molecular weight:164.2 g/molBenzyl (R)-(-)-Glycidyl Ether
CAS:Formula:C10H12O2Purity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:164.20(R)-Benzyl glycidyl ether
CAS:(R)-Benzyl glycidyl etherFormula:C10H12O2Purity:98+%Color and Shape: colourless to light yellow liquidMolecular weight:164.20g/molBenzyl (R)-(-)-glycidyl ether
CAS:Formula:C10H12O2Purity:98%Color and Shape:LiquidMolecular weight:164.20108000000002Ref: IN-DA007YHD
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