2-(4-Methylphenyl)-benzothiazole, with the CAS number 16112-21-3, is an organic compound characterized by its benzothiazole structure, which consists of a benzene ring fused to a thiazole ring. This compound features a methyl group attached to the para position of the phenyl group, enhancing its hydrophobic properties. It is typically a solid at room temperature and may exhibit a crystalline or powdery form. The presence of both aromatic and heterocyclic components contributes to its potential applications in various fields, including materials science and organic synthesis. The compound may also display interesting photophysical properties, making it a candidate for use in fluorescent materials or as a dye. Additionally, its chemical stability and reactivity can be influenced by the substituents on the aromatic rings, which may affect its interactions in biological systems or its utility in industrial applications. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

2-(4-Methylphenyl)-benzothiazole

16112-21-3: 2-(4-Methylphenyl)-1,3-Benzothiazole

2-(p-tolyl)-1,3-benzothiazole is a molecule that can transfer metal ions to devices. It has been shown to be efficient in ligand exchange reactions, giving high yields and good chemical stability. The synthetic reaction of 2-(p-tolyl)-1,3-benzothiazole generates ancillary ligands with high quantum efficiency. This molecule also has the ability to bind metal ions and chlorides because of its aromatic ring.

CAS 16112-21-3: 2-(4-Methylphenyl)-benzothiazole

2-(p-tolyl)-1,3-benzothiazole

Ref: 3D-RAA11221

2-(p-Tolyl)benzo[d]thiazole

Ref: 10-F436815

2-(p-tolyl)-1,3-benzothiazole

Ref: 54-OR480550

Benzothiazole, 2-(4-methylphenyl)-

Ref: IN-DA001S78