2,2,2-Trichloro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone
95%
- Product Code: 40509
CAS:
163220-69-7
| Molecular Weight: | 263.5100 g./mol | Molecular Formula: | C₉H₅Cl₃N₂O |
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| EC Number: | MDL Number: | MFCD18642801 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the preparation of pharmaceutical compounds, where it serves as a building block for active pharmaceutical ingredients (APIs). Its structure, featuring a trichloroethyl group and a pyrrolopyridine moiety, makes it a versatile reagent in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, it is employed in research settings for the development of novel chemical entities with potential therapeutic applications, such as kinase inhibitors or other biologically active molecules. Its reactivity and functional groups allow for further modifications, enabling the creation of diverse chemical libraries for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $130.07 |
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2,2,2-Trichloro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the preparation of pharmaceutical compounds, where it serves as a building block for active pharmaceutical ingredients (APIs). Its structure, featuring a trichloroethyl group and a pyrrolopyridine moiety, makes it a versatile reagent in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, it is employed in research settings for the development of novel chemical entities with potential therapeutic applications, such as kinase inhibitors or other biologically active molecules. Its reactivity and functional groups allow for further modifications, enabling the creation of diverse chemical libraries for drug discovery and development.
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