5-(2-FURYL)ISOXAZOLE-3-CARBOXYLIC ACID
5-(2-FURYL)ISOXAZOLE-3-CARBOXYLIC ACID Basic information
- Product Name:
- 5-(2-FURYL)ISOXAZOLE-3-CARBOXYLIC ACID
- Synonyms:
-
- 5-(2-furanyl)-3-isoxazolecarboxylic acid
- TIMTEC-BB SBB007153
- 5-(2-furyl)-3-isoxazolecarboxylic acid
- 5-(2-Furyl)isoxazole-3-carboxylic acid 95+%
- 109088
- 5-FURAN-2-YL-ISOXAZOLE-3-CARBOXYLIC ACID
- AKOS B022856
- AKOS PAO-1387
- CAS:
- 98434-06-1
- MF:
- C8H5NO4
- MW:
- 179.13
- Product Categories:
-
- Oxazole&Isoxazole
- Mol File:
- 98434-06-1.mol
5-(2-FURYL)ISOXAZOLE-3-CARBOXYLIC ACID Chemical Properties
- Melting point:
- 151 °C
- Boiling point:
- 418.4±35.0 °C(Predicted)
- Density
- 1.420±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- pka
- 3.33±0.10(Predicted)
- Appearance
- White to yellow Solid
- CAS DataBase Reference
- 98434-06-1(CAS DataBase Reference)
Safety Information
- Risk Statements
- 36/37/38
- Safety Statements
- 22-26-36/37/39
- HazardClass
- IRRITANT
- HS Code
- 2932190090
5-(2-FURYL)ISOXAZOLE-3-CARBOXYLIC ACID Usage And Synthesis
Synthesis
33545-40-3
98434-06-1
General procedure for the synthesis of 5-(2-furanyl)isoxazole-3-carboxylic acid from ethyl 5-(furan-2-yl)isoxazole-3-carboxylate: 1N aqueous lithium hydroxide solution (80 mL) was slowly added to a mixed solution of THF (130 mL) and methanol (25 mL) containing ethyl 5-(furan-2-yl)isoxazole-3-carboxylate (4.14 g). The reaction mixture was stirred at room temperature for 15 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was acidified by adding 1N hydrochloric acid to the residue until a solid precipitated. The solid product was collected by filtration and washed with distilled water. After drying, 3.22 g of 5-(2-furyl)isoxazole-3-carboxylic acid (yield: 90%) was obtained as a white solid. [178] 1H-NMR (acetone-d6, 200 MHz) δ: 7.90-7.86 (m, 1H), 7.19 (d, 1H), 7.00 (s, 1H), 6.77-6.73 (m, 1H).
References
[1] Patent: WO2009/5269, 2009, A2. Location in patent: Page/Page column 18
[2] Patent: US2009/131336, 2009, A1. Location in patent: Page/Page column 12
[3] Patent: WO2007/78113, 2007, A1. Location in patent: Page/Page column 36
[4] Gazzetta Chimica Italiana, 1958, vol. 88, p. 879,896
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