1-(4-Carboxyphenyl)-5-mercapto-1H-tetrazole
95%
- Product Code: 161213
CAS:
23249-95-8
| Molecular Weight: | 222.22 g./mol | Molecular Formula: | C₈H₆N₄O₂S |
|---|---|---|---|
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| Density: | Storage Condition: | Room temperature, stored in inert gas |
Product Description:
Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of sartan-class antihypertensive drugs such as valsartan and losartan. Its functional groups—carboxylic acid and thiol—enable coupling reactions and ring formation essential for building the tetrazole core found in many pharmaceuticals. Also employed in coordination chemistry as a ligand for metal ions due to its sulfur and nitrogen donor sites, making it useful in the development of metal-organic frameworks and sensors. Additionally, its reactivity allows modification for use in bioconjugation and drug delivery systems.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to light yellow powder to crystal |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | €27.93 |
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1-(4-Carboxyphenyl)-5-mercapto-1H-tetrazole
Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of sartan-class antihypertensive drugs such as valsartan and losartan. Its functional groups—carboxylic acid and thiol—enable coupling reactions and ring formation essential for building the tetrazole core found in many pharmaceuticals. Also employed in coordination chemistry as a ligand for metal ions due to its sulfur and nitrogen donor sites, making it useful in the development of metal-organic frameworks and sensors. Additionally, its reactivity allows modification for use in bioconjugation and drug delivery systems.
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