4-(Piperidin-4-yl)benzonitrile hydrochloride
95%
- Product Code: 46503
CAS:
162997-34-4
Molecular Weight: | 222.7139 g./mol | Molecular Formula: | C₁₂H₁₅ClN₂ |
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EC Number: | MDL Number: | MFCD08544124 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a piperidine ring and a benzonitrile group, makes it valuable for designing compounds targeting central nervous system disorders, particularly those involving neurotransmitter regulation. It is often employed in the creation of potential therapeutic agents for conditions like anxiety, depression, and neurodegenerative diseases. Additionally, its hydrochloride salt form enhances solubility, making it more suitable for experimental studies and drug formulation processes. Researchers also explore its use in developing receptor-specific ligands, aiding in the study of biochemical pathways and drug discovery efforts.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿7,416.00 |
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4-(Piperidin-4-yl)benzonitrile hydrochloride
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a piperidine ring and a benzonitrile group, makes it valuable for designing compounds targeting central nervous system disorders, particularly those involving neurotransmitter regulation. It is often employed in the creation of potential therapeutic agents for conditions like anxiety, depression, and neurodegenerative diseases. Additionally, its hydrochloride salt form enhances solubility, making it more suitable for experimental studies and drug formulation processes. Researchers also explore its use in developing receptor-specific ligands, aiding in the study of biochemical pathways and drug discovery efforts.
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