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2,4-Dichloro-5-thiazolecarboxylic acid

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2,4-Dichloro-5-thiazolecarboxylic acid Basic information

Product Name:
2,4-Dichloro-5-thiazolecarboxylic acid
Synonyms:
  • 5-Thiazolecarboxylic acid, 2,4-dichloro-
  • 2,4-Dichloro-5-thiazolecarboxylic acid
  • dichloro-1,3-thiazole-5-carboxylic acid
  • 2,4-DICHLORO-5-THIAZOLECARBOXYLIC ACID, 98% [62019-56-1
  • Thiazole-5-carboxylic acid, 2,4-dichloro-
CAS:
62019-56-1
MF:
C4HCl2NO2S
MW:
198.03
Mol File:
62019-56-1.mol
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2,4-Dichloro-5-thiazolecarboxylic acid Chemical Properties

Boiling point:
385.0±45.0 °C(Predicted)
Density 
1.824±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
1.05±0.28(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2934100090
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2,4-Dichloro-5-thiazolecarboxylic acid Usage And Synthesis

Uses

2,4-Dichloro-5-thiazolecarboxylic acid is an organic synthesis intermediate, widely used in the synthesis of thiazole compounds in the pharmaceutical and pesticide industries. It has multiple biological activities such as antibacterial, antifungal, anti-inflammatory, and antitumor.

Synthesis

92972-48-0

62019-56-1

General procedure for the synthesis of 2,4-dichloro-5-thiazole carboxylic acid from 2,4-dichlorothiazole-5-carboxaldehyde: To a mixed solution of 2,4-dichlorothiazole-5-carboxaldehyde (500 mg, 2.74 mmol) in tetrahydrofuran (18 ml) and water (12 ml) was added sulfonamide (346 mg, 3.56 mmol) and sodium chlorite (323 mg, 3.56 mmol) to an aqueous solution (2 ml). The reaction mixture was stirred at room temperature for 2 h. After completion of the reaction, it was diluted with ethyl acetate and washed with deionized water. The organic phase was separated and concentrated under reduced pressure to give the target product 2,4-dichloro-5-thiazolecarboxylic acid (440 mg, 88% yield) as a yellow solid.

References

[1] Patent: US2009/270456, 2009, A1. Location in patent: Page/Page column 8

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