Basic information Safety Supplier Related

ETHYL 3,4-DIMETHOXYPHENYLACETATE

Basic information Safety Supplier Related

ETHYL 3,4-DIMETHOXYPHENYLACETATE Basic information

Product Name:
ETHYL 3,4-DIMETHOXYPHENYLACETATE
Synonyms:
  • 3,4-dimethoxy-benzeneaceticaciethylester
  • Acetic acid, (3,4-dimethoxyphenyl)-, ethyl ester
  • Benzeneacetic acid, 3,4-dimethoxy-, ethyl ester
  • Ethyl dimethoxyphenylacetate
  • ETHYL 3,4-DIMETHOXYPHENYLACETATE
  • ETHYL 2-(3,4-DIMETHOXYPHENYL)ACETATE
  • HOMOVERATRIC ACID ETHYL ESTER
  • 3,4-Dimethoxyphenylacetic acid ethyl ester~Ethyl homoveratrate
CAS:
18066-68-7
MF:
C12H16O4
MW:
224.25
EINECS:
241-974-9
Product Categories:
  • Catechol Derivatives
  • Aromatic Esters
Mol File:
18066-68-7.mol
More
Less

ETHYL 3,4-DIMETHOXYPHENYLACETATE Chemical Properties

Boiling point:
191 °C
Density 
1.084±0.06 g/cm3(Predicted)
refractive index 
1.5180
Flash point:
159-160°C/4mm
storage temp. 
Sealed in dry,Room Temperature
form 
liquid
color 
Brown
BRN 
2697968
CAS DataBase Reference
18066-68-7(CAS DataBase Reference)
EPA Substance Registry System
Benzeneacetic acid, 3,4-dimethoxy-, ethyl ester (18066-68-7)
More
Less

Safety Information

TSCA 
Yes
HS Code 
2915390090

MSDS

  • Language:English Provider:ALFA
More
Less

ETHYL 3,4-DIMETHOXYPHENYLACETATE Usage And Synthesis

Synthesis

93-40-3

64-17-5

18066-68-7

In a typical reaction, 3,4-dimethoxyphenylacetic acid (332 g, 0.6 mol), ethanol (1.5-2 mol), and AMA 2:3 were mixed in a provided reaction glass tube equipped with a screw cap and magnetic stirrer until a wet mixture was formed. The reaction mixture was placed in a microwave reactor (Anton Parr Monowave 300) and irradiated at 80°C for 8 min or 120°C for 20 min. Upon completion of the reaction, the mixture was cooled, diluted with dichloromethane (41 mL), filtered by gravity and the filtrate was washed with dichloromethane. Subsequently, the filtrate was washed with saturated sodium carbonate solution and water. The organic layer was separated, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give ethyl 3,4-dimethoxyphenylacetate.

References

[1] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 4, p. 1586 - 1605
[2] Journal of Organic Chemistry, 2003, vol. 68, # 3, p. 1165 - 1167
[3] Synthetic Communications, 2014, vol. 44, # 16, p. 2386 - 2392
[4] Journal of Organic Chemistry, 2010, vol. 75, # 19, p. 6549 - 6562
[5] Tetrahedron, 1997, vol. 53, # 30, p. 10555 - 10564

ETHYL 3,4-DIMETHOXYPHENYLACETATESupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Email
product02@bidepharm.com