3,3′-Thiobis[6-hydroxybenzoic acid], with the CAS number 1820-99-1, is an organic compound characterized by its dual hydroxylated benzoic acid structure linked by a sulfur atom. This compound features two 6-hydroxybenzoic acid moieties, which contribute to its potential as a chelating agent and its ability to form hydrogen bonds due to the presence of hydroxyl groups. The thiobis linkage imparts unique properties, such as increased stability and potential for forming complexes with metal ions. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to its hydroxyl groups. The compound is of interest in various fields, including materials science and medicinal chemistry, due to its potential applications in drug formulation and as an antioxidant. Its chemical behavior can be influenced by pH and the presence of other functional groups, making it a versatile compound for research and industrial applications.

3,3′-Thiobis[6-hydroxybenzoic acid]

1820-99-1: 3,3'-Sulfanediylbis(6-Hydroxybenzoic Acid), 3,3′-Thiobis[6-hydroxybenzoic acid], 4,4′-Dihydroxy-3,3′-dicarboxydiphenyl sulfide, 5,5-Thiodisalicylic acid, Benzoic acid, 3,3′-thiobis[6-hydroxy-, Bis(3-carboxy-4-hydroxyphenyl) sulfide, Salicylic acid, 5,5′-thiodi-

5,5'-Thiodisalicylic Acid

5,5'-Thiodisalicylic Acid is a reactive functional group with a silver ion. This compound has a hydrochloric acid and hydroxy group that react to form a hydroxyl group with the proton. It also has a nitrogen atom, which can be found in the reactive acidic hydroxyl group of 5,5'-thiodisalicylic acid. The fatty acids are viscosity and carbonyl groups. 5,5'-Thiodisalicylic Acid is an organic compound that reacts with chloride to form patterns.

CAS 1820-99-1: 3,3′-Thiobis[6-hydroxybenzoic acid]

5,5'-Thiodisalicylic Acid

Ref: 3B-T0208

5,5'-Thiodisalicylic Acid

Ref: 3D-FT62679

Benzoic acid, 3,3'-thiobis[6-hydroxy-

Ref: IN-DA00239Q

5,5-Thiodisalicylic Acid

Ref: 54-OR1011761