(5,6-Dihydro-4H-[1,3]thiazin-2-yl)-(4-ethoxy-phenyl)-amine, with the CAS number 100253-53-0, is a chemical compound characterized by its thiazine ring structure, which contributes to its unique properties. This compound features a thiazine moiety that is fused with an ethoxy-substituted phenyl group, indicating the presence of both nitrogen and sulfur atoms in its ring structure. The thiazine ring typically imparts certain stability and reactivity characteristics, making it of interest in medicinal chemistry. The ethoxy group enhances its lipophilicity, potentially influencing its bioavailability and interaction with biological systems. Additionally, the amine functional group suggests the potential for hydrogen bonding and reactivity with electrophiles. Overall, this compound may exhibit interesting pharmacological properties, making it a candidate for further research in drug development or as a biochemical probe. However, specific biological activity, solubility, and stability would require empirical investigation to fully understand its potential applications.

(5,6-DIHYDRO-4H-[1,3]THIAZIN-2-YL)-(4-ETHOXY-PHENYL)-AMINE

100253-53-0: (5,6-Dihydro-4H-[1,3]thiazin-2-yl)-(4-ethoxy-phenyl)-amine, with the CAS number 100253-53-0, is a chemical compound characterized by its thiazine ring structure, which contributes to its unique properties. This compound features a thiazine moiety that is fused with an ethoxy-substituted phenyl group, indicating the presence of both nitrogen and sulfur atoms in its ring structure. The thiazine ring typically imparts certain stability and reactivity characteristics, making it of interest in medicinal chemistry. The ethoxy group enhances its lipophilicity, potentially influencing its bioavailability and interaction with biological systems. Additionally, the amine functional group suggests the potential for hydrogen bonding and reactivity with electrophiles. Overall, this compound may exhibit interesting pharmacological properties, making it a candidate for further research in drug development or as a biochemical probe. However, specific biological activity, solubility, and stability would require empirical investigation to fully understand its potential applications.

CAS 100253-53-0

(5,6-DIHYDRO-4H-[1,3]THIAZIN-2-YL)-(4-ETHOXY-PHENYL)-AMINE

N-(4-ethoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine

Ref: IN-DA0001E9

N-(4-Ethoxyphenyl)-5,6-dihydro-4H-1,3-thiazin-2-amine

Ref: 3D-AEA25353