Basic information Safety Supplier Related

METHYL 2,3-DICHLOROBENZOATE

Basic information Safety Supplier Related

METHYL 2,3-DICHLOROBENZOATE Basic information

Product Name:
METHYL 2,3-DICHLOROBENZOATE
Synonyms:
  • METHYL 2,3-DICHLOROBENZOATE
  • 2,3-DICHLOROBENZOIC ACID METHYL ESTER
  • RARECHEM AL BF 0205
  • Methyl 2,3-dichlorobenzoate,97%
  • 2,3-Dichlorobenzoic methylester
  • Methyl 2,3-dichlorobenzoate,98+%
  • Benzoic acid, 2,3-dichloro-, Methyl ester
  • 2,3-dichloro-benzoicacimethylester
CAS:
2905-54-6
MF:
C8H6Cl2O2
MW:
205.04
Product Categories:
  • Aromatic Esters
Mol File:
2905-54-6.mol
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METHYL 2,3-DICHLOROBENZOATE Chemical Properties

Melting point:
33-38 °C
Boiling point:
294.45°C (rough estimate)
Density 
1.36
refractive index 
1.5537
Flash point:
110 °C
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
EPA Substance Registry System
Benzoic acid, 2,3-dichloro-, methyl ester (2905-54-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
HS Code 
29163900

MSDS

  • Language:English Provider:ACROS
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METHYL 2,3-DICHLOROBENZOATE Usage And Synthesis

Chemical Properties

white crystals

Synthesis

50-45-3

2905-54-6

a) 2,3-Dichlorobenzoic acid (100 g, 0.526 mol) was dissolved in methanol (1 L) and concentrated sulfuric acid (20 mL) was added slowly. The reaction mixture was stirred under reflux conditions for 12 hours. After completion of the reaction, it was cooled to room temperature and concentrated under reduced pressure to remove most of the solvent. The residue was diluted with ethyl acetate (1 L) and water (100 mL) and the organic layer was separated. The organic phase was washed sequentially with saturated sodium bicarbonate solution and brine and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to afford methyl 2,3-dichlorobenzoate (99 g, 92% yield) as a white solid.1H NMR (300 MHz, CDCl3) δ ppm: 3.95 (s, 3H), 7.27 (t, J = 7.8 Hz, 1H), 7.60 (dd, J = 1.8, 7.8 Hz, 1H), 7.66 (dd, J = 1.8, 7.8 Hz, 1H).

References

[1] Patent: WO2013/28263, 2013, A1. Location in patent: Page/Page column 78
[2] Patent: US9096605, 2015, B2
[3] Patent: EP459830, 1991, A1

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