Imidazo[2,1-b][1,3]benzothiazol-2-ylmethanol is a heterocyclic compound characterized by its unique fused ring structure, which combines imidazole and benzothiazole moieties. This compound typically exhibits properties associated with both aromatic and heteroaromatic systems, including stability and potential biological activity. The presence of the hydroxymethyl group (-CH2OH) contributes to its solubility in polar solvents and may enhance its reactivity, particularly in forming derivatives or participating in chemical reactions. Compounds of this type are often investigated for their pharmacological properties, including antimicrobial and anticancer activities, due to the presence of nitrogen and sulfur atoms in their structure, which can interact with biological targets. Additionally, the compound may exhibit fluorescence properties, making it of interest in various applications, including materials science and biochemistry. Its specific applications and behavior in biological systems would depend on further studies and characterization, including its interaction with enzymes or receptors.

IMIDAZO[2,1-B][1,3]BENZOTHIAZOL-2-YLMETHANOL

114095-02-2: Imidazo[2,1-b][1,3]benzothiazol-2-ylmethanol is a heterocyclic compound characterized by its unique fused ring structure, which combines imidazole and benzothiazole moieties. This compound typically exhibits properties associated with both aromatic and heteroaromatic systems, including stability and potential biological activity. The presence of the hydroxymethyl group (-CH2OH) contributes to its solubility in polar solvents and may enhance its reactivity, particularly in forming derivatives or participating in chemical reactions. Compounds of this type are often investigated for their pharmacological properties, including antimicrobial and anticancer activities, due to the presence of nitrogen and sulfur atoms in their structure, which can interact with biological targets. Additionally, the compound may exhibit fluorescence properties, making it of interest in various applications, including materials science and biochemistry. Its specific applications and behavior in biological systems would depend on further studies and characterization, including its interaction with enzymes or receptors.

CAS 114095-02-2

IMIDAZO[2,1-B][1,3]BENZOTHIAZOL-2-YLMETHANOL

(Imidazo[2,1-b]benzothiazol-2-yl)methanol

Ref: IN-DA000AJA

(Imidazo[2,1-b][1,3]benzothiazol-2-yl)methanol

Ref: 54-OR3587

Imidazo[2,1-b][1,3]benzothiazol-2-ylmethanol

Ref: 10-F023701