Atomfair n-Methyl-3-(2-methylthiazol-4-yl)aniline C11H12N2S

Description n-Methyl-3-(2-methylthiazol-4-yl)aniline (CAS No. 1448189-30-7) is a high-purity organic compound with the molecular formula C11H12N2S and IUPAC name N-methyl-3-(2-methyl-1,3-thiazol-4-yl)aniline . This specialized chemical features a thiazole ring linked to an aniline derivative, making it a valuable intermediate for pharmaceutical and agrochemical research. With a molecular weight of 204.29 g/mol, it is supplied as a solid with ??95% purity (HPLC), ensuring consistency for synthetic applications. Suitable for use in cross-coupling reactions, heterocyclic synthesis, and medicinal chemistry studies. Store under inert conditions at 2-8??C to maintain stability.

Description

Description

n-Methyl-3-(2-methylthiazol-4-yl)aniline (CAS No. 1448189-30-7) is a high-purity organic compound with the molecular formula C11H12N2S and IUPAC name N-methyl-3-(2-methyl-1,3-thiazol-4-yl)aniline. This specialized chemical features a thiazole ring linked to an aniline derivative, making it a valuable intermediate for pharmaceutical and agrochemical research. With a molecular weight of 204.29 g/mol, it is supplied as a solid with ??95% purity (HPLC), ensuring consistency for synthetic applications. Suitable for use in cross-coupling reactions, heterocyclic synthesis, and medicinal chemistry studies. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 1448189-30-7
  • Molecular Formula: C11H12N2S
  • Molecular Weight: 204.29
  • Exact Mass: 204.07211956
  • Monoisotopic Mass: 204.07211956
  • IUPAC Name: N-methyl-3-(2-methyl-1,3-thiazol-4-yl)aniline
  • SMILES: CC1=NC(=CS1)C2=CC(=CC=C2)NC
  • Synonyms: n-Methyl-3-(2-methylthiazol-4-yl)aniline, 1339729-30-4, N-methyl-3-(2-methyl-1,3-thiazol-4-yl)aniline, AKOS012392278, CS-0282276

Application

n-Methyl-3-(2-methylthiazol-4-yl)aniline serves as a key building block in the synthesis of biologically active molecules, particularly in drug discovery for kinase inhibitors and antimicrobial agents. Its thiazole-aniline structure is utilized in the development of fluorescent probes for cellular imaging studies. Researchers employ this compound in palladium-catalyzed coupling reactions to construct complex heterocyclic scaffolds.

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