3-Hydroxythiophene-2-carboxylic acid
3-Hydroxythiophene-2-carboxylic acid Basic information
- Product Name:
- 3-Hydroxythiophene-2-carboxylic acid
- Synonyms:
-
- 3-Hydroxythiophene-2-carboxylic acid
- 3-Hydroxy-2-thiophenecarboxylic acid
- 2-Carboxy-3-hydroxythiophene, 3-Hydroxy-2-thenoic acid
- 3-Hydroxythiophene-2-carboxylic acid 97%
- 2-(dihydroxymethylidene)-3-thiophenone
- 2-Thiophenecarboxylic acid, 3-hydroxy-
- 3-Hydroxythiophene-2-carboxylic acid ISO 9001:2015 REACH
- CAS:
- 5118-07-0
- MF:
- C5H4O3S
- MW:
- 144.15
- Product Categories:
-
- Carboxylic Acids
- Thiophenes & Benzothiophenes
- Carboxylic Acids
- Thiophenes & Benzothiophenes
- Mol File:
- 5118-07-0.mol
3-Hydroxythiophene-2-carboxylic acid Chemical Properties
- Melting point:
- 108 °C(Solv: acetone (67-64-1))
- Boiling point:
- 326.4±27.0 °C(Predicted)
- Density
- 1.603±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- form
- crystalline powder
- pka
- 3.79±0.10(Predicted)
- color
- Brown/grey
Safety Information
- Hazard Codes
- Xi
- HS Code
- 2934999090
3-Hydroxythiophene-2-carboxylic acid Usage And Synthesis
Uses
3-Hydroxythiophene-2-carboxylic acid (cas# 5118-07-0) is a useful research chemical. This compound is useful because furoates and thenoates inhibit pyruvate dehydrogenase kinase 2 allosterically by binding to its pyruvate regulatory site.
Synthesis
186588-88-5
5118-07-0
General procedure for the synthesis of 3-hydroxythiophene-2-carboxylic acid from 3-benzyloxythiophene-2-carboxylic acid: a) 3-benzyloxythiophene-2-carboxylic acid (1.0 g) was hydrogenated with 10% palladium-carbon catalyst (1.8 g) in a mixture of ethanol (150 mL) and 2N hydrochloric acid (4.5 mL) for 2 hours at 45 psi hydrogen pressure. Upon completion of the reaction, the mixture was filtered through a layer of diatomaceous earth and the filtrate was concentrated under vacuum to afford 3-hydroxythiophene-2-carboxylic acid (600 mg, 98% yield) as an off-white solid product. The product was characterized by 1H NMR (300 MHz, CDCl3): δ 6.78 (d, 1H), 7.49 (d, 1H). Mass spectrometry (APCI) showed m/z=145 (M+1).LC/MS analysis showed a retention time of 1.15 min.
References
[1] Patent: WO2007/1225, 2007, A1. Location in patent: Page/Page column 16
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