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Ethyl methoxyacetate

Basic information Safety Supplier Related

Ethyl methoxyacetate Basic information

Product Name:
Ethyl methoxyacetate
Synonyms:
  • Methoxyacetic acid, ethyl ester
  • ETHYL METHOXYACETATE
  • ETHYL-3-OXABUTANOATE
  • ETHYL 2-METHOXYACETATE
  • Acetic acid, methoxy-, ethyl ester
  • 2-Methoxyacetic acid ethyl ester
  • Ethyl Methoxyacetate, 98% 10GR
  • Ethyl methoxyacetate,98%
CAS:
3938-96-3
MF:
C5H10O3
MW:
118.13
EINECS:
223-521-7
Product Categories:
  • Building Blocks
  • C2 to C5
  • Carbonyl Compounds
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Acetics acid and esters
  • C2 to C5
  • Esters
Mol File:
3938-96-3.mol
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Ethyl methoxyacetate Chemical Properties

Boiling point:
44-45.5 °C/9 mmHg (lit.)
Density 
1.007 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.401(lit.)
Flash point:
115 °F
storage temp. 
Flammables area
form 
clear liquid
color 
Colorless to Almost colorless
Water Solubility 
Slightly soluble in water.
BRN 
1744761
LogP
0.475 (est)
CAS DataBase Reference
3938-96-3(CAS DataBase Reference)
NIST Chemistry Reference
Acetic acid, methoxy-, ethyl ester(3938-96-3)
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Safety Information

Risk Statements 
10
Safety Statements 
16-24/25
RIDADR 
UN 3272 3/PG 3
WGK Germany 
3
HazardClass 
3
PackingGroup 
III
HS Code 
29189900

MSDS

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Ethyl methoxyacetate Usage And Synthesis

Chemical Properties

clear colorless liquid

Uses

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.

Uses

Ethyl methoxyacetate was used:

  • as acyl donor during the preparation of enantiomers of several phenylethylamines
  • as acylation reagent for the aminolysis of 1-phenylethanamine
  • in an industrial, lipase-catalysed kinetic resolution of primary amine

Application

Ethyl methoxyacetate was used:
as acyl donor during the preparation of enantiomers of several phenylethylamines
as acylation reagent for the aminolysis of 1-phenylethanamine
in an industrial, lipase-catalysed kinetic resolution of primary amine

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