922730-86-7
![5-(Methoxy-d<sub>3</sub>)-1H-benzo[d]imidazole-2-thiol Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-w699846.gif "5-(Methoxy-d<sub>3</sub>)-1H-benzo[d]imidazole-2-thiol Chemical Structure")
922730-86-7
Chemical Structure
5-(Methoxy-d3)-1H-benzo[d]imidazole-2-thiol
- CAS No.: 922730-86-7
- Formula:C8H5D3N2OS
- Molecular Weight:183.25
IUPAC Name: 5-(methoxy-d3)-1H-benzo[d]imidazole-2-thiol
InChIKey: KOFBRZWVWJCLGM-FIBGUPNXSA-N
SMILES: SC1=NC2=C(C=CC(OC([2H])([2H])[2H])=C2)N1
Biological Activity: 5-(Methoxy-d3)-1H-benzo[d]imidazole-2-thiol is the deuterated-labeled 5-Methoxy-2-benzimidazolethiol (HY-W008378). 5-Methoxy-2-benzimidazolethiol is a benzimidazole derivative. 5-Methoxy-2-benzimidazolethiol can serve as a ligand for transition metal complexes[1][2].
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5-(Methoxy-d3)-1H-benzo[d]imidazole-2-thiol | 5-(Methoxy-d3)-1H-benzo[d]imidazole-2-thiol is the deuterated-labeled 5-Methoxy-2-benzimidazolethiol (HY-W008378). 5-Methoxy-2-benzimidazolethiol is a benzimidazole derivative. 5-Methoxy-2-benzimidazolethiol can serve as a ligand for transition metal complexes. | |||||||||||||||||||||
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5-Methoxy-2-benzimidazolethiol (Standard) | ≥98% | 5-Methoxy-2-benzimidazolethiol (Standard) is the analytical standard of 5-Methoxy-2-benzimidazolethiol (HY-W008378). This product is intended for research and analytical applications. 5-Methoxy-2-benzimidazolethiol is a benzimidazole derivative. 5-Methoxy-2-benzimidazolethiol can serve as a ligand for transition metal complexes. | ||||||||||||||||||||
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5-Methoxy-2-benzimidazolethiol-d3 | 5-Methoxy-2-benzimidazolethiol-d3 is the deuterated-labeled 5-Methoxy-2-benzimidazolethiol (HY-W008378). 5-Methoxy-2-benzimidazolethiol is a benzimidazole derivative. 5-Methoxy-2-benzimidazolethiol can serve as a ligand for transition metal complexes. | |||||||||||||||||||||
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5-Methoxy-2-benzimidazolethiol | 99.55% | 5-Methoxy-2-benzimidazolethiol is a benzimidazole derivative. 5-Methoxy-2-benzimidazolethiol can serve as a ligand for transition metal complexes. | ||||||||||||||||||||
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References
- [1]. Hu J, et al. Triiodide Attacks the Organic Cation in Hybrid Lead Halide Perovskites: Mechanism and Suppression. Advanced materials (Deerfield Beach, Fla.). 2023 Oct;35(40):e2303373.
- [2]. Manjuraj T, et al. Metal complexes of quinolin‑8‑yl [(5‑methoxy‑1H‑benzimidazol‑2‑yl) sulfanyl]acetate: Spectral, XRD, thermal, cytotoxic, molecular docking and biological evaluation. J Mol Struct. 2017;1148:231‑237.
