CAS 56133-37-0
:4-Isothiazolecarboxylic acid, methyl ester
Description:
4-Isothiazolecarboxylic acid, methyl ester is an organic compound characterized by its isothiazole ring structure, which features a five-membered heterocyclic ring containing both sulfur and nitrogen atoms. This compound typically exhibits properties associated with carboxylic acid derivatives, including moderate polarity due to the presence of the ester functional group. It is generally soluble in polar organic solvents and may have limited solubility in water. The methyl ester form suggests that it can undergo hydrolysis to yield the corresponding carboxylic acid, which may exhibit different reactivity and biological activity. Compounds like this are often of interest in medicinal chemistry and agricultural applications due to their potential biological activities, including antimicrobial and herbicidal properties. Additionally, the presence of the isothiazole moiety can contribute to unique chemical reactivity, making it a valuable scaffold in drug design. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C5H5NO2S
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Found 2 products.
Methyl 1,2-thiazole-4-carboxylate
CAS:<p>Methyl 1,2-thiazole-4-carboxylate is a benzyl derivative that has been shown to have the ability to repair DNA. This compound is a pharmacological agent that has been shown to have anti-inflammatory and anti-tumour properties. Methyl 1,2-thiazole-4-carboxylate is also an inhibitor of alkyltransferase and inactivates purines and guanines. It is metabolized by the enzyme methyltransferase which modifies it to methyl 2,3-thiazole carboxylate. The stereochemistry of this molecule can be determined by focusing on the methyl group on carbon number 2 or 3.</p>Formula:C5H5NO2SPurity:Min. 95%Molecular weight:143.17 g/mol
