Benzothiazole
Benzothiazole (CAS No.: 95-16-9) is a naturally occurring heterocyclic scaffold widely utilized in biomedical research as a versatile fragment for molecular design and chemical biology investigations. As a privileged structure in medicinal chemistry, it serves as a core framework for the development and optimization of small molecules with diverse bioactivities, including reported anticancer, antimicrobial, antidiabetic, anti-inflammatory, antiviral, and antileishmanial effects observed in experimental systems. Mechanistically, benzothiazole-derived compounds have been shown to interact with multiple biological targets and pathways, such as enzyme modulation, receptor binding, and interference with cellular signaling cascades, depending on structural substitution patterns, and certain derivatives have demonstrated affinity for β-amyloid aggregates, supporting their application in imaging-related research. In vitro studies of benzothiazole-based molecules typically report activity in the nanomolar to micromolar range across various biochemical and cell-based assays, although potency is highly context-dependent. This compound is therefore frequently employed as a building block in drug discovery programs, enabling scaffold hopping, molecular hybridization, and structure–activity relationship studies, and is commonly applied in screening platforms, cell-based models, and preclinical exploratory systems, where experimental concentrations or dosing regimens are determined by specific research objectives and assay conditions.
| Physical Appearance | A liquid |
| Storage | -20°C |
| M.Wt | 135.18 |
| Cas No. | 95-16-9 |
| Formula | C7H5NS |
| Solubility | ≥24.3 mg/mL in DMSO; ≥16.9 mg/mL in EtOH; ≥4.77 mg/mL in H2O |
| Chemical Name | benzo[d]thiazole |
| Canonical SMILES | C12=CC=CC=C1SC=N2 |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







