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Ethyl 2-Chlorobenzoate

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Ethyl 2-Chlorobenzoate Basic information

Product Name:
Ethyl 2-Chlorobenzoate
Synonyms:
  • ETHYL 2-CHLOROBENZOATE
  • ETHYL O-CHLOROBENZOATE
  • RARECHEM AL BI 0018
  • O-CHLOROBENZOIC ACID ETHYL ESTER
  • ETHYL 2-CHLOROBENZOATE 98%
  • Ethyl 2-chlorobenzoate, 98+%
  • 2-CHLOROBENZOIC ACID ETHYL ESTER
  • ETHYL 2-CHLOROBENZOA
CAS:
7335-25-3
MF:
C9H9ClO2
MW:
184.62
EINECS:
230-842-6
Product Categories:
  • Chlorine Compounds
  • C8 to C9
  • Carbonyl Compounds
  • Esters
  • Aromatic Esters
  • Benzoic acid
  • Acids & Esters
Mol File:
7335-25-3.mol
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Ethyl 2-Chlorobenzoate Chemical Properties

Boiling point:
241-243 °C(lit.)
Density 
1.18 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.523(lit.)
Flash point:
>230 °F
storage temp. 
Store at room temperature
form 
clear liquid
color 
Colorless to Almost colorless
Specific Gravity
1.180
BRN 
2207359
CAS DataBase Reference
7335-25-3(CAS DataBase Reference)
EPA Substance Registry System
Benzoic acid, 2-chloro-, ethyl ester (7335-25-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
HS Code 
29163990

MSDS

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Ethyl 2-Chlorobenzoate Usage And Synthesis

Chemical Properties

Clear colorless to pale yellow liquid

Synthesis

383-63-1

898768-95-1

7335-25-3

288310-94-1

GENERAL PROCEDURE: In a dry Schlenk tube, sodium hydride (6.0 mmol) was stirred with ethyl trifluoroacetate (6.0 mmol) in tetrahydrofuran (5 mL) for 10 minutes at room temperature under argon protection. Subsequently, a solution of enolizable ketone (5.0 mmol) in tetrahydrofuran (5 mL) was slowly added dropwise to the above mixture at 0°C and under argon atmosphere. The reaction solution was stirred at a set temperature for 2 to 6 hours before being cooled again to 0°C and the reaction was quenched with 6 mL of a 1 mol/L hydrochloric acid solution. After continued stirring for 15 minutes, the mixture was neutralized with saturated sodium bicarbonate solution. After conventional post-treatment steps, the residue was purified by silica gel column chromatography to give the target product trifluoromethyl alkyl ketone.

References

[1] Tetrahedron, 2014, vol. 70, # 31, p. 4668 - 4674

Ethyl 2-Chlorobenzoate Preparation Products And Raw materials

Raw materials

Preparation Products

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