5-(2-Methyl-1,3-thiazol-4-yl)indoline, with the CAS number 144340-48-7, is an organic compound characterized by its unique structural features, which include an indoline moiety fused with a thiazole ring. This compound typically exhibits properties associated with both heterocyclic and aromatic compounds, contributing to its potential biological activity. The presence of the thiazole ring suggests that it may participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Additionally, the methyl group on the thiazole enhances its lipophilicity, potentially influencing its solubility and permeability in biological systems. Such characteristics make it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. The compound's stability, reactivity, and interaction with biological targets can vary based on environmental conditions, such as pH and temperature. Overall, 5-(2-methyl-1,3-thiazol-4-yl)indoline represents a class of compounds that may have significant implications in drug discovery and development.

5-(2-METHYL-1,3-THIAZOL-4-YL)INDOLINE

144340-48-7: 5-(2-Methyl-1,3-thiazol-4-yl)indoline, with the CAS number 144340-48-7, is an organic compound characterized by its unique structural features, which include an indoline moiety fused with a thiazole ring. This compound typically exhibits properties associated with both heterocyclic and aromatic compounds, contributing to its potential biological activity. The presence of the thiazole ring suggests that it may participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Additionally, the methyl group on the thiazole enhances its lipophilicity, potentially influencing its solubility and permeability in biological systems. Such characteristics make it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. The compound's stability, reactivity, and interaction with biological targets can vary based on environmental conditions, such as pH and temperature. Overall, 5-(2-methyl-1,3-thiazol-4-yl)indoline represents a class of compounds that may have significant implications in drug discovery and development.

CAS 144340-48-7

5-(2-METHYL-1,3-THIAZOL-4-YL)INDOLINE

5-(2-methyl-1,3-thiazol-4-yl)-2,3-dihydro-1H-indole

Ref: IN-DA001JCX

5-(2-Methyl-1,3-thiazol-4-yl)-2,3-dihydro-1H-indole

Ref: 3D-UFA34048