(S)-Diethyl 2-(5-(methylamino)thiophene-2-carboxamido)pentanedioate
≥95%
- Product Code: 51392
CAS:
112889-02-8
| Molecular Weight: | 342.41 g./mol | Molecular Formula: | C₁₅H₂₂N₂O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09750956 | |
| Melting Point: | Boiling Point: | 519.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring a thiophene ring and amino groups, makes it valuable for developing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Researchers often employ it in the design and optimization of drug candidates, especially in areas like neurology or oncology, where specific interactions with biological targets are crucial. Additionally, its ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening and efficacy studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $37.07 |
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| 0.250 | 10-20 days | $74.13 |
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(S)-Diethyl 2-(5-(methylamino)thiophene-2-carboxamido)pentanedioate
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring a thiophene ring and amino groups, makes it valuable for developing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Researchers often employ it in the design and optimization of drug candidates, especially in areas like neurology or oncology, where specific interactions with biological targets are crucial. Additionally, its ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening and efficacy studies.
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