CymitQuimica logo

CAS 13139-47-4

:

2-acetylthiazole-4-carboxylic acid

Description:
2-Acetylthiazole-4-carboxylic acid is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen. This compound features an acetyl group and a carboxylic acid functional group, contributing to its reactivity and potential applications in various chemical reactions. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the carboxylic acid group. The thiazole moiety can participate in various chemical transformations, making this compound of interest in synthetic organic chemistry. Additionally, its derivatives may possess biological activity, which could be explored for pharmaceutical applications. The compound's molecular structure allows for potential interactions with biological targets, making it a candidate for further research in medicinal chemistry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices.
Formula:C6H5NO3S
InChI:InChI=1/C6H5NO3S/c1-3(8)5-7-4(2-11-5)6(9)10/h2H,1H3,(H,9,10)
Synonyms:
  • 2-Atca
  • 2-acetyl-1,3-thiazole-4-carboxylic acid
  • 4-Thiazolecarboxylic acid, 2-acetyl-
  • 2-Acetylthiazole-4-carboxylic acid
Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
  • 2-Acetylthiazole-4-carboxylic acid

    CAS:
    Formula:C6H5NO3S
    Molecular weight:171.1738

    Ref: IN-DA000W2G

    ne
    To inquire
  • 2-Acetyl-1,3-thiazole-4-carboxylic acid

    CAS:
    2-Acetyl-1,3-thiazole-4-carboxylic acid is a carbonyl compound that is structurally related to other algicides. It has been shown to be effective against marine bacteria and organisms, including algae, bacteria and fungi. The 2-acetyl derivative of 1,3-thiazole has been found to have the highest activity among the derivatives tested. The chemical structure of this compound is similar to that of methyl ester and can be easily hydrolyzed by alkaline solutions. 2-Acetyl-1,3-thiazole-4-carboxylic acid also reacts with oxygen in air to form an unstable oxide which decomposes into water and carbon dioxide. This characteristic makes it suitable for use as an algicide because it can be easily decomposed by sunlight or UV light.
    Formula:C6H5NO3S
    Purity:Min. 95%
    Molecular weight:171.18 g/mol

    Ref: 3D-NAA13947

    1g
    1,049.00€
    100mg
    423.00€