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Thermo Scientific Chemicals
Ethyl methoxyacetate, 98%
CAS: 3938-96-3 | C5H10O3 | 118.132 g/mol
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Catalog number A18770.09
also known as A18770-09
Price (EUR)
44,50
Each
Quantity:
10 g
Price (EUR)
44,50
Each
Chemical Identifiers
CAS3938-96-3
IUPAC Nameethyl 2-methoxyacetate
Molecular FormulaC5H10O3
InChI KeyJLEKJZUYWFJPMB-UHFFFAOYSA-N
SMILESCCOC(=O)COC
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Specifications
Specification Sheet
Specification SheetFormLiquid
Refractive Index1.3985-1.4025 @ 20?C
Appearance (Color)Clear colorless
Assay (GC)≥97.5%
Ethyl methoxyacetate was used as acyl donor during the preparation of enantiomers of several phenylethylamines, as acylation reagent for the aminolysis of 1-phenylethanamine and used in an industrial, lipase-catalyzed kinetic resolution of primary amine.
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.
Applications
Ethyl methoxyacetate was used as acyl donor during the preparation of enantiomers of several phenylethylamines, as acylation reagent for the aminolysis of 1-phenylethanamine and used in an industrial, lipase-catalyzed kinetic resolution of primary amine.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
Ethyl methoxyacetate was used as acyl donor during the preparation of enantiomers of several phenylethylamines, as acylation reagent for the aminolysis of 1-phenylethanamine and used in an industrial, lipase-catalyzed kinetic resolution of primary amine.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Lourdes Muñoz; Anna M Rodriguez; Gloria Rosell; M Pilar Bosch; Angel Guerrero. Enzymatic enantiomeric resolution of phenylethylamines structurally related to amphetamine. Organic & Biomolecular Chemistry, 2011, 9 (23), 8171-8177.
- Maria Cammenberg; Karl Hult; Seongsoon Park. Molecular basis for the enhanced lipase-catalyzed N-acylation of 1-phenylethanamine with methoxyacetate. ChemBioChem, 2006, 7(11), 1745-1749.