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3-Hydroxythiophene-2-carboxylic acid

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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
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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
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Safety Information

Hazard Codes 
Xi
HS Code 
2934999090
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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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