6-(4-Bromophenyl)piperidin-2-one
95%
- Product Code: 49454
CAS:
267880-78-4
| Molecular Weight: | 254.1231 g./mol | Molecular Formula: | C₁₁H₁₂BrNO |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring a bromophenyl group and a piperidinone ring, makes it a valuable building block for the development of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the synthesis of compounds with potential anticancer properties, as the bromophenyl moiety can enhance binding affinity to specific biological targets. Researchers also explore its use in creating novel materials with unique electronic properties, particularly in the development of organic semiconductors. Its versatility in chemical reactions, including coupling and cyclization processes, further broadens its application in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,791.00 |
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6-(4-Bromophenyl)piperidin-2-one
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring a bromophenyl group and a piperidinone ring, makes it a valuable building block for the development of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the synthesis of compounds with potential anticancer properties, as the bromophenyl moiety can enhance binding affinity to specific biological targets. Researchers also explore its use in creating novel materials with unique electronic properties, particularly in the development of organic semiconductors. Its versatility in chemical reactions, including coupling and cyclization processes, further broadens its application in medicinal chemistry and material science.
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