2-Carbethoxy-2-(carbethoxymethyl)-1-cyclopentanone
95%
- Product Code: 83074
CAS:
41301-66-0
| Molecular Weight: | 242.27 g./mol | Molecular Formula: | C₁₂H₁₈O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00665204 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the production of complex cyclic structures, particularly in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in constructing molecules with specific biological activities. Additionally, it is employed in the development of fine chemicals and specialty materials, where its reactivity and stability are advantageous. Researchers often use it in cyclization reactions to create five-membered rings, which are common motifs in many active compounds. Its application extends to the field of medicinal chemistry, where it contributes to the design and synthesis of potential drug candidates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿9,450.00 |
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| 250mg | 10-20 days | ฿17,550.00 |
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| 1g | 10-20 days | ฿35,100.00 |
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2-Carbethoxy-2-(carbethoxymethyl)-1-cyclopentanone
This compound is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the production of complex cyclic structures, particularly in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in constructing molecules with specific biological activities. Additionally, it is employed in the development of fine chemicals and specialty materials, where its reactivity and stability are advantageous. Researchers often use it in cyclization reactions to create five-membered rings, which are common motifs in many active compounds. Its application extends to the field of medicinal chemistry, where it contributes to the design and synthesis of potential drug candidates.
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