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