CAS 14527-42-5

2-Thiazolecarboxylicacid, ethyl ester

Description:

2-Thiazolecarboxylic acid, ethyl ester, is an organic compound characterized by its thiazole ring structure, which incorporates both sulfur and nitrogen atoms. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic ethyl ester group. The presence of the carboxylic acid functional group contributes to its acidic properties, while the ethyl ester moiety enhances its reactivity in various chemical reactions, including esterification and hydrolysis. This compound is often utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety data indicates that it should be handled with care, as it may cause irritation to skin and eyes. Proper storage in a cool, dry place away from incompatible substances is recommended to maintain its stability.

Formula: C₆H₇NO₂S

Synonyms:

• 2-(Ethoxycarbonyl)thiazole
• Ethyl 1,3-thiazole-2-carboxylate
• Ethyl thiazole-2-carboxylate
• 2-Thiazolecarboxylic acid, ethyl ester

2-Thiazolecarboxylic acid, ethyl ester

CAS: 14527-42-5

Formula: C₆H₇NO₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 157.1903

Ref: IN-DA001KQI

Ethyl thiazole-2-carboxylate

CAS: 14527-42-5

Ethyl thiazole-2-carboxylate

Purity: 97%

Molecular weight: 157.19g/mol

Ref: 54-OR964945

Thiazole-2-carboxylic acid ethyl ester

CAS: 14527-42-5

Thiazole-2-carboxylic acid ethyl ester is a synthetic compound that is used as a model for peroxides and as a substrate in the study of carbonyl chemistry. It has been shown to react with benzene, yielding an alpha-hydroxybenzylidene ketone. The heterocycle can be converted to the corresponding carboxylic acid by dehydrogenation with hydrogen peroxide or sodium perborate. The yields of this reaction are dependent on the substituent effects of the heterocycle. Thiazole-2-carboxylic acid ethyl ester reacts with serine protease and amide in an enzyme assay. Kinetic data for this reaction are available in the literature.

Formula: C₆H₇NO₂S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 157.19 g/mol

Ref: 3D-FT139140

Ethyl thiazole-2-carboxylate

CAS: 14527-42-5

Formula: C₆H₇NO₂S

Purity: 95%

Molecular weight: 157.19

Ref: 10-F220276