2-Mercapto-1H-benzo[d]imidazol-5-ol
97%
- Product Code: 85157
CAS:
92806-98-9
| Molecular Weight: | 166.20 g./mol | Molecular Formula: | C₇H₆N₂OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04117895 | |
| Melting Point: | Boiling Point: | 422.2 °C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, inert gas storage |
Product Description:
Used in the synthesis of pharmaceuticals, particularly in the development of drugs targeting oxidative stress and inflammation. Acts as a key intermediate in the production of antioxidants and anti-inflammatory agents.
Employed in the manufacturing of rubber chemicals, where it serves as a vulcanization accelerator, enhancing the durability and elasticity of rubber products.
Utilized in the field of organic synthesis as a building block for complex molecules, especially in the creation of heterocyclic compounds with potential biological activity.
Applied in research laboratories as a reagent for studying thiol-based reactions and mechanisms, contributing to advancements in chemical and biochemical studies.
Also finds use in the development of corrosion inhibitors, protecting metal surfaces from degradation in industrial environments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $74.59 |
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| 0.250 | 10-20 days | $124.31 |
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| 1.000 | 10-20 days | $308.74 |
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2-Mercapto-1H-benzo[d]imidazol-5-ol
Used in the synthesis of pharmaceuticals, particularly in the development of drugs targeting oxidative stress and inflammation. Acts as a key intermediate in the production of antioxidants and anti-inflammatory agents.
Employed in the manufacturing of rubber chemicals, where it serves as a vulcanization accelerator, enhancing the durability and elasticity of rubber products.
Utilized in the field of organic synthesis as a building block for complex molecules, especially in the creation of heterocyclic compounds with potential biological activity.
Applied in research laboratories as a reagent for studying thiol-based reactions and mechanisms, contributing to advancements in chemical and biochemical studies.
Also finds use in the development of corrosion inhibitors, protecting metal surfaces from degradation in industrial environments.
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