1,3-Benzenedimethanethiol, also known as 1,3-dimercaptobenzene, is an organic compound characterized by the presence of two thiol (-SH) groups attached to a benzene ring at the 1 and 3 positions. This compound is a colorless to pale yellow liquid with a strong, unpleasant odor reminiscent of rotten eggs or garlic, typical of thiols. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic benzene ring. The presence of thiol groups imparts significant reactivity, allowing it to participate in various chemical reactions, including oxidation and formation of disulfides. 1,3-Benzenedimethanethiol is used in organic synthesis and may serve as a building block for more complex molecules. Additionally, it has potential applications in materials science and as a ligand in coordination chemistry. Safety precautions are necessary when handling this compound, as thiols can be toxic and irritating to the skin and respiratory system.

1,3-benzenedimethanethiol

41563-69-3: 3-(Mercaptomethyl)Phenyl Methanethiol, O-Xylene DithiOl, Benzene-1,3-Diyldimethanethiol,  , 

1,3-Benzenedimethol is a molecule that is used in supramolecular chemistry. The molecule has been studied for its ability to prevent the formation of a monolayer on gold. It has been shown to have a crystalline structure and low energy. 1,3-Benzenedimethanethiol has also been studied for its use as an optical probe and its application in prostate cancer cells. This molecule can react with water vapor, which may contribute to its optical properties. Lastly, 1,3-benzenedimethanethiol has been studied for its use as an electrochemical probe in the study of the kinetics of hydrogen fluoride.

CAS 41563-69-3: 1,3-benzenedimethanethiol

1,3-Benzenedimethanethiol

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1,3-Benzenedimethanethiol

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1,3-Benzenedimethanethiol

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1,3-Benzenedimethanethiol

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