N-Methyl-2-benzothiazolamine 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 nitrogen atom of the amine functional group, contributing to its unique properties. It is typically a solid at room temperature and may exhibit a range of colors depending on its purity and form. N-Methyl-2-benzothiazolamine is known for its applications in various fields, including as a chemical intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It may also possess biological activity, making it of interest in medicinal chemistry. The compound is soluble in organic solvents but has limited solubility in water, which is a common characteristic of many aromatic amines. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Proper storage and handling procedures are essential to mitigate any potential hazards associated with this chemical.

N-Methyl-2-benzothiazolamine

16954-69-1: 2-(Methylamino)benzothiazole, 2-(N-Methylamino)benzothiazole, 2-Benzothiazolamine, N-methyl-, 2-Benzothiazolamine, N-methyl- (9CI), 2-Methylaminobenzothiazole, Benzothiazol-2-ylmethylamine, Benzothiazole, 2-(methylamino)-, Brn 0122355, N-(2-Benzothiazolyl)methylamine, N-Methyl-2-benzothiazolamine, N-methyl-1,3-benzothiazol-2-amine,  4-27-00-04826 (Beilstein Handbook Reference),  N-Methylbenzothiazol-2-amine

N-Methyl-1,3-benzothiazol-2-amine

N-Methylbenzo[d]thiazol-2-amine

N-Methyl-1,3-benzothiazol-2-amine is a molecule that belongs to the class of isothiocyanates. It can be synthesized by reacting 2-chlorobenzothiazole with primary amines in the presence of a nonpolar solvent. This method is efficient and can provide high yields for this molecule. N-Methyl-1,3-benzothiazol-2-amine has been shown to inhibit the uptake of pesticides by plants. The mechanism is not well understood but it may involve vibrational interactions with molecules in the plant cell membrane or chemical interactions with other molecules in the plant cell. This molecule also has nitrogen atoms and mass spectrometric techniques have shown that it has an nmr spectrum.

CAS 16954-69-1: N-Methyl-2-benzothiazolamine

N-Methyl-1,3-benzothiazol-2-amine

Ref: 54-OR943526

N-Methylbenzo[d]thiazol-2-amine

Ref: 10-F217885

N-Methyl-1,3-benzothiazol-2-amine

Ref: 3D-RAA95469