Methyl 3-aminothieno[3,2-c]pyridine-2-carboxylate
≥95%
- Product Code: 117825
CAS:
111042-92-3
Molecular Weight: | 208.24 g./mol | Molecular Formula: | C₉H₈N₂O₂S |
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EC Number: | MDL Number: | MFCD08234760 | |
Melting Point: | Boiling Point: | 393.8±37.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting therapeutic areas such as central nervous system disorders, inflammation, and infectious diseases. Its unique thienopyridine structure makes it a valuable building block for creating molecules with potential pharmacological properties. Researchers often employ it in the design and optimization of drug candidates, leveraging its chemical framework to enhance drug efficacy and selectivity. Additionally, it is used in academic and industrial laboratories for studying structure-activity relationships and developing novel medicinal agents.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,260.00 |
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0.250 | 10-20 days | ฿5,660.00 |
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1.000 | 10-20 days | ฿14,480.00 |
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Methyl 3-aminothieno[3,2-c]pyridine-2-carboxylate
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting therapeutic areas such as central nervous system disorders, inflammation, and infectious diseases. Its unique thienopyridine structure makes it a valuable building block for creating molecules with potential pharmacological properties. Researchers often employ it in the design and optimization of drug candidates, leveraging its chemical framework to enhance drug efficacy and selectivity. Additionally, it is used in academic and industrial laboratories for studying structure-activity relationships and developing novel medicinal agents.
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