1-(2-Fluorobenzyl)piperazine
96%
- Product Code: 86497
CAS:
89292-78-4
Molecular Weight: | 194.25 g./mol | Molecular Formula: | C₁₁H₁₅FN₂ |
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EC Number: | MDL Number: | MFCD02256027 | |
Melting Point: | Boiling Point: | 93 - 96 ℃ at 0.3 百帕 - lit. | |
Density: | 1.170 g/mL at 25 ℃(lit.) | Storage Condition: | room temperature |
Product Description:
Primarily utilized in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting the central nervous system, where it can be incorporated into drugs designed to interact with neurotransmitter receptors. Additionally, it has been explored in the creation of potential therapeutic agents for psychiatric and neurological disorders, such as anxiety and depression, due to its ability to modulate receptor activity. The fluorobenzyl group enhances the binding affinity and metabolic stability of the resulting compounds, making it a crucial component in drug discovery and development processes.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless to Tan Liquid |
PURITY | 95.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,750.00 |
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5.000 | 10-20 days | ฿5,870.00 |
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1-(2-Fluorobenzyl)piperazine
Primarily utilized in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting the central nervous system, where it can be incorporated into drugs designed to interact with neurotransmitter receptors. Additionally, it has been explored in the creation of potential therapeutic agents for psychiatric and neurological disorders, such as anxiety and depression, due to its ability to modulate receptor activity. The fluorobenzyl group enhances the binding affinity and metabolic stability of the resulting compounds, making it a crucial component in drug discovery and development processes.
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