N-[(1R,2R)-2-aMino-1,2-bis(4-Methoxyphenyl)ethyl]-4-Methyl-BenzenesulfonaMide
98%
- Product Code: 70692
CAS:
852212-99-8
| Molecular Weight: | 426.52854 g./mol | Molecular Formula: | C₂₃H₂₆N₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, away from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both amino and sulfonamide groups, makes it a valuable precursor in the development of pharmaceutical agents, particularly those targeting enzymatic pathways. It is often employed in the design and synthesis of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, which are crucial in drug development to ensure specificity and reduce side effects. Researchers also explore its use in studying molecular interactions and binding affinities due to its unique structural properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,690.00 |
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| 1.000 | 10-20 days | ฿3,100.00 |
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| 5.000 | 10-20 days | ฿14,880.00 |
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N-[(1R,2R)-2-aMino-1,2-bis(4-Methoxyphenyl)ethyl]-4-Methyl-BenzenesulfonaMide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both amino and sulfonamide groups, makes it a valuable precursor in the development of pharmaceutical agents, particularly those targeting enzymatic pathways. It is often employed in the design and synthesis of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, which are crucial in drug development to ensure specificity and reduce side effects. Researchers also explore its use in studying molecular interactions and binding affinities due to its unique structural properties.
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