Basic information Safety Supplier Related

ETHYL 3-CHLOROBENZOATE

Basic information Safety Supplier Related

ETHYL 3-CHLOROBENZOATE Basic information

Product Name:
ETHYL 3-CHLOROBENZOATE
Synonyms:
  • Benzoic acid, m-chloro-, ethyl ester
  • Ethyl m-chlorobenzoate
  • ETHYL 3-CHLOROBENZOATE
  • 3-CHLOROBENZOIC ACID ETHYL ESTER
  • NSC 67339
  • RARECHEM AL BI 0056
  • Ethyl 3-chlorobenzoate, 98+%
  • Ethyl 3-Chlorobenzoate >
CAS:
1128-76-3
MF:
C9H9ClO2
MW:
184.62
EINECS:
214-441-3
Product Categories:
  • Aromatic Esters
  • Benzoic acid
  • Acids & Esters
  • Chlorine Compounds
Mol File:
1128-76-3.mol
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ETHYL 3-CHLOROBENZOATE Chemical Properties

Boiling point:
118-120°C 13mm
Density 
1,186 g/cm3
refractive index 
1.5220
Flash point:
118-120°C/13mm
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
BRN 
2045877
CAS DataBase Reference
1128-76-3(CAS DataBase Reference)
EPA Substance Registry System
Benzoic acid, 3-chloro-, ethyl ester (1128-76-3)
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Safety Information

Safety Statements 
24/25
HS Code 
2916399090

MSDS

  • Language:English Provider:ALFA
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ETHYL 3-CHLOROBENZOATE Usage And Synthesis

Synthesis

75-00-3

535-80-8

1128-76-3

Under stirring conditions, 3-chlorobenzoic acid (1.00 mmol), chloroethane (1.20 mmol), and IL-1 (0.30 mmol) were sequentially added to a two-necked flask containing 6 mL of 50% aqueous ethanol solution. Subsequently, the temperature of the reaction system was raised to 70 °C and maintained at this temperature in a water bath. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reactor was cooled to room temperature. The reaction mixture was diluted with 10 mL of water and extracted with ethyl acetate (3 x 5 mL). The organic phases were combined, dried over anhydrous Na2SO4 and filtered, and the filtrate was concentrated in a rotary evaporator to give ethyl m-chlorobenzoate. The catalyst was dried under vacuum at 80 °C for 6 h after removing the solvent and could be recycled for the next round of reaction. All esterification products need to be further purified by column chromatography.

References

[1] Catalysis Letters, 2017, vol. 147, # 11, p. 2764 - 2771

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