| Identification | Back Directory | [Name]
5-Thiazolecarboxylic acid, 2,4-dichloro- | [CAS]
62019-56-1 | [Synonyms]
2,4-Dichloro-5-thiazolecarboxylic acid
dichloro-1,3-thiazole-5-carboxylic acid
5-Thiazolecarboxylic acid, 2,4-dichloro-
Thiazole-5-carboxylic acid, 2,4-dichloro-
2,4-DICHLORO-5-THIAZOLECARBOXYLIC ACID, 98% [62019-56-1 | [Molecular Formula]
C4HCl2NO2S | [MDL Number]
MFCD09909676 | [MOL File]
62019-56-1.mol | [Molecular Weight]
198.03 |
| Chemical Properties | Back Directory | [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 |
| Hazard Information | Back Directory | [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]
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 |
|
|