(3S,5S)-5-(1S,3S)-1-Azido-3-[4-methoxy-3-(3-methoxypropoxy)benzy l]-4-methylpentyl-3-isopropyldihydro-2(3H)-furanone
98%
- Product Code: 47957
CAS:
324763-46-4
| Molecular Weight: | 461.59 g./mol | Molecular Formula: | C₂₅H₃₉N₃O₅ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a key intermediate in the synthesis of complex molecules. Its unique structure, featuring azido and methoxypropoxy groups, makes it valuable for developing targeted drug candidates, particularly in the design of enzyme inhibitors or receptor modulators. The azide functionality allows for further chemical modifications through click chemistry, enabling the creation of diverse derivatives for biological screening. It is often employed in the development of therapeutics for conditions such as cardiovascular diseases or metabolic disorders, where precise molecular interactions are critical. Additionally, its stereochemistry plays a significant role in enhancing the selectivity and efficacy of the resulting drug molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $405.04 |
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(3S,5S)-5-(1S,3S)-1-Azido-3-[4-methoxy-3-(3-methoxypropoxy)benzy l]-4-methylpentyl-3-isopropyldihydro-2(3H)-furanone
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a key intermediate in the synthesis of complex molecules. Its unique structure, featuring azido and methoxypropoxy groups, makes it valuable for developing targeted drug candidates, particularly in the design of enzyme inhibitors or receptor modulators. The azide functionality allows for further chemical modifications through click chemistry, enabling the creation of diverse derivatives for biological screening. It is often employed in the development of therapeutics for conditions such as cardiovascular diseases or metabolic disorders, where precise molecular interactions are critical. Additionally, its stereochemistry plays a significant role in enhancing the selectivity and efficacy of the resulting drug molecules.
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