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CAS:5118-06-9 | Methyl 3-hydroxythiophene-2-carboxylate

CAS:5118-06-9 | Methyl 3-hydroxythiophene-2-carboxylate

Name:Methyl 3-hydroxythiophene-2-carboxylate
CAS:5118-06-9
MF:C6H6O3S
MW:158.18 g/mol
Purity:97%
EINECS:692-439-5
Appearance:White to Orange to Green powder to crystal
Package: 5g,25g,100g,500g,1kg,25kg
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Product Introduction

Introduction and application of CAS 5118-06-9 | Methyl 3-hydroxythiophene-2-carboxylate

Methyl 3-hydroxythiophene-2-carboxylate is an organic compound consisting of a methyl group attached to a thiophene ring. It is a precursor to the drug amiloride, which is used to treat hypertension and edema.

 

The compound can be formed by the reaction of hydrogen chloride with an alcohol in alkaline conditions. It can also be synthesized from 3-chlorothiophene-2-carboxylic acid and methanol in dilute hydrochloric acid.

 

In addition, it can be prepared by chlorination of methyltetrahydrothiophene-2-carboxylic acid in the presence of copper(II) oxide as a catalyst. The compound has been decarboxylated at 200°C and then reacted with chloroform under refluxing conditions to produce amiloride.

 

Synonyms:

methyl 3-hydroxy-thiophene-2-carboxylate;

3-oxy-2-carbomethoxy-thiophene;

3-Hydroxythiophene-2-carboxylic acid methyl ester;

3-Hydroxy-2-thiophenecarboxylic Acid Methyl Ester;

2-methoxycarbonyl-3-hydroxy-thiophene;

2-carbomethoxy-3-hydroxy-thiophene;

Methyl 3-hydroxy-2-thiophenecarboxylate;

Methyl 3-Hydroxythiophene-2-Carboxylate;

 

Specification of CAS 5118-06-9 | Methyl 3-hydroxythiophene-2-carboxylate

ITEMS

SPECIFICATION

CAS

5118-06-9

MF

C6H6O3S

MW

158.18

Boiling point

107-109°C 13mm

Density

1.372±0.06 g/cm3(Predicted)

Water solubility

 

Slightly soluble in water.

acidity coefficient(pKa)

9.47±0.10(Predicted)

 

Package and transportation of Introduction and application of CAS 5118-06-9 | Methyl 3-hydroxythiophene-2-carboxylate

Package: 5g,25g,100g,500g,1kg,25kg

Transportation: by courier/ by air/ by sea

 

product-763-725

Related Articles of CAS 5118-06-9 | Methyl 3-hydroxythiophene-2-carboxylate

Reactions of methyl 3‐hydroxythiophene‐2‐carboxylate. Part 4. Synthesis of methyl 5‐azolyl‐3‐hydroxythiophene‐2‐carboxylates

C Corral, MB El‐Ashmawy, J Lissavetzky… - Journal of …, 1987 - Wiley Online Library

The indirect introduction of an azolyl group in position 5 of compound 1 by an easy two‐step

procedure taking place at room temperature is described. A similar procedure yields the 4‐…

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