1-(4-Bromo-2-methylbenzoyl)piperazine
95%
- Product Code: 39354
CAS:
1156842-50-0
| Molecular Weight: | 283.16 g./mol | Molecular Formula: | C₁₂H₁₅BrN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12096627 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a piperazine ring and a bromo-methylbenzoyl group, makes it a versatile building block for developing compounds with potential therapeutic applications. It is often employed in the design and synthesis of ligands that target specific receptors in the central nervous system, contributing to the development of drugs for neurological and psychiatric disorders. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery and optimization.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿4,500.00 |
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| 0.100 | 10-20 days | ฿10,800.00 |
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1-(4-Bromo-2-methylbenzoyl)piperazine
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a piperazine ring and a bromo-methylbenzoyl group, makes it a versatile building block for developing compounds with potential therapeutic applications. It is often employed in the design and synthesis of ligands that target specific receptors in the central nervous system, contributing to the development of drugs for neurological and psychiatric disorders. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery and optimization.
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