1,3-Benzothiazole-2-carboxylic acid is an organic compound characterized by its bicyclic structure, which includes a benzene ring fused to a thiazole ring. This compound features a carboxylic acid functional group (-COOH) at the 2-position of the thiazole ring, contributing to its acidic properties. It is typically a white to off-white solid that is soluble in polar solvents such as water and alcohols, while being less soluble in non-polar solvents. The compound exhibits various chemical reactivity due to the presence of both the carboxylic acid and the thiazole moiety, making it useful in synthetic organic chemistry and as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, 1,3-benzothiazole derivatives are known for their biological activities, including antimicrobial and antifungal properties. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety measures should be observed when working with this substance in a laboratory setting.

1,3-Benzothiazole-2-carboxylic acid

3622-04-6: Benzo[D]Thiazole-2-Carboxylic Acid

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Sodium 1,3-benzothiazole-2-carboxylate is an amide that belongs to the molecule class of organic compounds. This molecule has a hydroxyl group, which is a reactive functional group that can be used to form hydrogen bonds with other molecules. It also has an enzyme activity and can be used as a cancer therapeutic agent. Sodium 1,3-benzothiazole-2-carboxylate inhibits estrogen receptor modulators and may have potential for treating autoimmune diseases and cancer. It is synthesized by reacting picolinic acid with sodium thiocyanate in the presence of methanol.

CAS 3622-04-6: 1,3-Benzothiazole-2-carboxylic acid

1,3-Benzothiazole-2-carboxylic acid

Ref: 3D-DAA62204

Sodium 1,3-benzothiazole-2-carboxylate

Ref: 3D-FS124189

1,3-Benzothiazole-2-carboxylic acid

Ref: 54-OR23086

2-Benzothiazolecarboxylic acid

Ref: IN-DA00I76G