Basic information Safety Supplier Related

Methyl 5-thiazolecarboxylate

Basic information Safety Supplier Related

Methyl 5-thiazolecarboxylate Basic information

Product Name:
Methyl 5-thiazolecarboxylate
Synonyms:
  • Methyl 1,3-thiazole-5-carboxylate 98%
  • methyl 1,3-thiazole-5-carboxylate
  • METHYL 5-THIAZOLECARBOXYLATE
  • METHYL THIAZOLE-5-CARBOXYLATE
  • RARECHEM AL BF 1261
  • 5-Thiazolecarboxylic acid, methyl ester
  • Thiazole-5-carboxylic acid methyl ester
  • Methyl 5-thiazolecar
CAS:
14527-44-7
MF:
C5H5NO2S
MW:
143.16
Product Categories:
  • Building Blocks
  • C3 to C7
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • New Products for Chemical Synthesis
  • blocks
  • Carboxes
  • Thiazoles
Mol File:
14527-44-7.mol
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Methyl 5-thiazolecarboxylate Chemical Properties

Melting point:
68-69°C
Boiling point:
87-90°C (10 mmHg)
Density 
1.45
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
0.80±0.10(Predicted)
Appearance
Off-white to light yellow Solid
CAS DataBase Reference
14527-44-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39
Hazard Note 
Harmful
HS Code 
2934100090
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Methyl 5-thiazolecarboxylate Usage And Synthesis

Synthesis

6633-61-0

14527-44-7

The general procedure for the synthesis of methyl 5-thiazolecarboxylate from methyl 2-aminothiazole-5-carboxylate was as follows: a mixture of 2.25 g of isoamyl nitrite with 10 mL of dioxane was stirred at 80 °C under nitrogen protection. Subsequently, a 20 mL dioxane solution containing 1.23 g of methyl 2-aminothiazole-5-carboxylate (g-3) was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was refluxed for 2 hours. After the reaction was completed, it was cooled to room temperature and diluted by adding 30 mL of ethyl acetate. The organic phase was washed with saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography to give 0.54 g (48% yield) of the target product methyl 5-thiazolecarboxylate (g-4).

References

[1] Patent: WO2003/97616, 2003, A1. Location in patent: Page/Page column 26

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