2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID
2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID Basic information
- Product Name:
- 2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID
- Synonyms:
-
- 5-Carboxy-2-methyl-4-(trifluoromethyl)-1,3-thiazole
- 5-Thiazolecarboxylic acid, 2-Methyl-4-(trifluoroMethyl)-
- 2-Methyl-4-(trifluoromethyl)
- e-5-carboxyL
- -4-(trifL
- 2-Methyl-4-(trifluoromethyl)thiazole-5-carboxylicaci
- 2-methyl-4-(trifluoromethyl)- 5-Thiazolecarboxylic acid
- 2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CAR
- CAS:
- 117724-63-7
- MF:
- C6H4F3NO2S
- MW:
- 211.16
- EINECS:
- 809-864-0
- Product Categories:
-
- Building Blocks
- Thiazole
- Mol File:
- 117724-63-7.mol
2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID Chemical Properties
- Melting point:
- 186~187℃
- Boiling point:
- 285.5±40.0 °C(Predicted)
- Density
- 1.570±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 1.97±0.36(Predicted)
- color
- White to Light yellow to Light orange
- InChI
- InChI=1S/C6H4F3NO2S/c1-2-10-4(6(7,8)9)3(13-2)5(11)12/h1H3,(H,11,12)
- InChIKey
- REKJPVUFKQYMHW-UHFFFAOYSA-N
- SMILES
- S1C(C(O)=O)=C(C(F)(F)F)N=C1C
2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID Usage And Synthesis
Uses
2-Methyl-4-(trifluoromethyl)thiazole-5-carboxylic Acid can be used to prepare a fungicidal mixture.
Synthesis
117724-62-6
117724-63-7
General procedure for the synthesis of 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylic acid from ethyl 2-methyl-4-trifluoromethyl-5-thiazolecarboxylate: 115 g of ethyl 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylate (0.102 mol) was dissolved in ethyl acetate at room temperature, and 50 g of 40% sodium hydroxide solution was added dropwise slowly into a reaction vessel with controlled The acceleration of the drop was controlled to maintain the temperature of the reaction system below 40 °C. After the dropwise addition, the reaction temperature was maintained and stirring was continued for 60 minutes. After the reaction was completed, the organic phase was separated and 10% hydrochloric acid solution was slowly added to the organic phase to adjust the pH value of the system to ≤2, at which time a large amount of solid precipitate precipitated. The precipitate was filtered and the filter cake was washed twice with 10% hydrochloric acid solution and subsequently dried in a vacuum oven. The resulting 2-methyl-4-(trifluoromethyl)thiazole-5-carboxylic acid was a light yellow solid with a yield of 21.5 g, a purity of 98.8% and a reaction yield of 98.70%.
References
[1] Journal of Fluorine Chemistry, 2004, vol. 125, # 9, p. 1287 - 1290
[2] Patent: US4837242, 1989, A
[3] Patent: CN103145639, 2016, B. Location in patent: Paragraph 0035; 0036; 0037
[4] Journal of Heterocyclic Chemistry, 2017, vol. 54, # 6, p. 3395 - 3402
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2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID(117724-63-7)Related Product Information
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