Basic information Safety Supplier Related

METHYL 3-CHLOROPHENYLACETATE

Basic information Safety Supplier Related

METHYL 3-CHLOROPHENYLACETATE Basic information

Product Name:
METHYL 3-CHLOROPHENYLACETATE
Synonyms:
  • (3-CHLORO-PHENYL)-ACETIC ACID METHYL ESTER
  • METHYL 3-CHLOROPHENYLACETATE
  • Methyl 3-chlorophenylacetate,99%
  • Methyl 3-chlorophenylacetate,98%
  • Methyl3-chlorophenylacetat
  • Methyl 3-chlorophenylacetate, 98% 25GR
  • Methyle3-chlorophenylacetate
  • Methyl 2-(3-chlorophenyl)acetate
CAS:
53088-68-9
MF:
C9H9ClO2
MW:
184.62
Product Categories:
  • Aromatic Esters
Mol File:
53088-68-9.mol
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METHYL 3-CHLOROPHENYLACETATE Chemical Properties

Boiling point:
120-121℃ (9 Torr)
Density 
1.197±0.06 g/cm3 (20 ºC 760 Torr)
refractive index 
1.5225-1.5245
Flash point:
108.8±15.8℃
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
color 
Clear colorless to light yellow
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
24/25-36/37/39
HS Code 
29153900

MSDS

  • Language:English Provider:ACROS
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METHYL 3-CHLOROPHENYLACETATE Usage And Synthesis

Chemical Properties

clear slightly yellowish liquid

Synthesis

67-56-1

1878-65-5

53088-68-9

GENERAL METHOD: Thionyl chloride (1.06 mL, 14.63 mmol) was added slowly and dropwise to a solution of 3-chlorophenylacetic acid (1 g, 4.877 mmol) in methanol (10 mL) at 0 °C. The reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, the solvent was removed by evaporation under reduced pressure. The residue was dissolved in a solvent mixture of ethyl acetate and water. The aqueous phase was extracted with ethyl acetate and the combined organic phases were washed with aqueous sodium bicarbonate. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give methyl m-chlorophenylacetate (6a-f).

References

[1] Tetrahedron, 1997, vol. 53, # 38, p. 13149 - 13164
[2] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2843 - 2866
[3] Journal of Medicinal Chemistry, 2001, vol. 44, # 17, p. 2701 - 2706
[4] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 4, p. 1679 - 1693
[5] Tetrahedron Letters, 2003, vol. 44, # 2, p. 331 - 334

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