Basic information Safety Supplier Related

Ethyl 2-methylthiazole-5-carboxylate

Basic information Safety Supplier Related

Ethyl 2-methylthiazole-5-carboxylate Basic information

Product Name:
Ethyl 2-methylthiazole-5-carboxylate
Synonyms:
  • 5-(Ethoxycarbonyl)-2-methyl-1,3-thiazole
  • ETHYL 2-METHYL-5-THIAZOLECARBOXYLATE
  • ETHYL 2-METHYL-THIAZOLE-5-CARBOXYLATE
  • 2-METHYL-THIAZOLE-5-CARBOXYLIC ACID ETHYL ESTER
  • ETHYL2-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
  • 2-methyl-5-(carbethoxy)thiazole
  • 5-Thiazolecarboxylicacid, 2-Methyl-, ethyl ester
CAS:
79836-78-5
MF:
C7H9NO2S
MW:
171.22
Product Categories:
  • Building Blocks
  • Thiazole series
  • Esters
  • Thiazoles, Isothiazoles &Benzothiazoles
  • Thiazole
  • Thiazoles, Isothiazoles & Benzothiazoles
Mol File:
79836-78-5.mol
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Ethyl 2-methylthiazole-5-carboxylate Chemical Properties

Boiling point:
117-120 °C
Density 
1.198±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
1.61±0.10(Predicted)
Appearance
Colorless to yellow Liquid
InChIKey
ORCQTMZHDQSNOJ-UHFFFAOYSA-N
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Safety Information

HS Code 
2934100090
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Ethyl 2-methylthiazole-5-carboxylate Usage And Synthesis

Synthesis Reference(s)

Journal of the American Chemical Society, 104, p. 4461, 1982 DOI: 10.1021/ja00380a022

Synthesis

62-55-5

33142-21-1

79836-78-5

To a stirred solution of ethyl 2-chloro-3-oxopropanoate (5.0 g, 33 mmol) in benzene (50 mL) under argon protection was added thioacetamide (2.5 g, 33 mmol) and the mixture was heated to reflux. After 4 h, the reaction mixture was cooled to room temperature, diluted with water (50 mL) and neutralized with saturated sodium bicarbonate solution to pH 7. Subsequently, the reaction mixture was extracted with ethyl acetate and the organic phases were combined and washed sequentially with water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. Purification by silica gel column chromatography (eluent: heptane/ethyl acetate, 0 to 50% gradient) afforded ethyl 2-methylthiazole-5-carboxylate (2.68 g, 47% yield) as a yellow liquid. Mass spectrometry (MS) analysis showed: m/e = 172.0 [M + H]+.

References

[1] Journal of the American Chemical Society, 1982, vol. 104, # 16, p. 4461 - 4465
[2] Patent: WO2010/127974, 2010, A1. Location in patent: Page/Page column 43
[3] Patent: WO2018/53157, 2018, A1. Location in patent: Page/Page column 108; 109
[4] Patent: WO2018/160878, 2018, A1. Location in patent: Page/Page column 278-279
[5] Journal of Chemical Research, 2011, vol. 35, # 5, p. 313 - 316

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