2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole
98%
- Product Code: 206887
CAS:
117977-21-6
| Molecular Weight: | 343.44 g./mol | Molecular Formula: | C₁₈H₂₁N₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 120.5-121.5°C | Boiling Point: | 546.4°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily as an intermediate in the synthesis of proton pump inhibitors (PPIs), this compound plays a key role in the development of medications that reduce stomach acid production. It is especially valuable in the manufacturing of drugs used to treat gastroesophageal reflux disease (GERD), peptic ulcers, and other acid-related gastrointestinal disorders. Due to its ability to selectively target the H+/K+ ATPase enzyme system in the gastric parietal cells, derivatives made from this chemical contribute to long-lasting acid suppression. Its structure allows for optimized stability and bioavailability in final drug formulations, making it a preferred choice in the design of effective anti-ulcer medications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿320.00 |
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| 5.000 G | 10-20 days | ฿1,040.00 |
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| 25.000 G | 10-20 days | ฿3,190.00 |
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| 100.000 G | 10-20 days | ฿10,410.00 |
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2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole
Used primarily as an intermediate in the synthesis of proton pump inhibitors (PPIs), this compound plays a key role in the development of medications that reduce stomach acid production. It is especially valuable in the manufacturing of drugs used to treat gastroesophageal reflux disease (GERD), peptic ulcers, and other acid-related gastrointestinal disorders. Due to its ability to selectively target the H+/K+ ATPase enzyme system in the gastric parietal cells, derivatives made from this chemical contribute to long-lasting acid suppression. Its structure allows for optimized stability and bioavailability in final drug formulations, making it a preferred choice in the design of effective anti-ulcer medications.
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