(S)-methyl 2-(picolinamido)butanoate
95%
- Product Code: 38608
CAS:
1353863-79-2
| Molecular Weight: | 222.24 g./mol | Molecular Formula: | C₁₁H₁₄N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06660120 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.152±0.06 g/cm3(Predicted) | Storage Condition: | 2-8 °C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex molecules. It is often employed in the development of pharmaceuticals, where its chiral structure is valuable for creating enantiomerically pure drugs. The compound’s picolinamide group enhances its ability to interact with biological targets, making it useful in the design of enzyme inhibitors or receptor modulators. Additionally, it can be used in research settings to study stereoselective reactions, aiding in the development of new synthetic methodologies. Its ester functionality also allows for further chemical modifications, making it a versatile building block in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,148.00 |
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| 0.250 | 10-20 days | ฿9,360.00 |
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| 1.000 | 10-20 days | ฿18,720.00 |
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(S)-methyl 2-(picolinamido)butanoate
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex molecules. It is often employed in the development of pharmaceuticals, where its chiral structure is valuable for creating enantiomerically pure drugs. The compound’s picolinamide group enhances its ability to interact with biological targets, making it useful in the design of enzyme inhibitors or receptor modulators. Additionally, it can be used in research settings to study stereoselective reactions, aiding in the development of new synthetic methodologies. Its ester functionality also allows for further chemical modifications, making it a versatile building block in medicinal chemistry and drug discovery.
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