1-(2-(4-Bromo-2-chlorophenoxy)ethyl)-4-methylpiperazine
95%
- Product Code: 123760
CAS:
401801-83-0
Molecular Weight: | 333.65 g./mol | Molecular Formula: | C₁₃H₁₈BrClN₂O |
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EC Number: | MDL Number: | MFCD28400524 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of bioactive molecules. It serves as a key intermediate in the creation of compounds that exhibit potential therapeutic effects, such as antipsychotic or antihistamine properties. Its structure, featuring a piperazine ring and halogenated phenoxy group, makes it a versatile building block for designing drugs targeting the central nervous system. Additionally, it may be explored in the development of agrochemicals, where its structural components could contribute to the formulation of herbicides or pesticides. The compound’s reactivity and functional groups allow for further chemical modifications, enabling researchers to optimize its efficacy and specificity for various applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿20,700.00 |
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1.000 | 10-20 days | ฿27,000.00 |
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5.000 | 10-20 days | ฿54,000.00 |
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1-(2-(4-Bromo-2-chlorophenoxy)ethyl)-4-methylpiperazine
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of bioactive molecules. It serves as a key intermediate in the creation of compounds that exhibit potential therapeutic effects, such as antipsychotic or antihistamine properties. Its structure, featuring a piperazine ring and halogenated phenoxy group, makes it a versatile building block for designing drugs targeting the central nervous system. Additionally, it may be explored in the development of agrochemicals, where its structural components could contribute to the formulation of herbicides or pesticides. The compound’s reactivity and functional groups allow for further chemical modifications, enabling researchers to optimize its efficacy and specificity for various applications.
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