(4-(1H-Pyrazol-1-yl)phenyl)methanamine hydrochloride
97%
- Product Code: 73981
CAS:
1107632-13-2
| Molecular Weight: | 209.68 g./mol | Molecular Formula: | C₁₀H₁₂ClN₃ |
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| EC Number: | MDL Number: | MFCD11505500 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific receptors or enzymes in therapeutic applications. Its structure, featuring a pyrazole moiety, makes it valuable in designing compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it is explored in the development of small-molecule inhibitors for treating neurological disorders due to its ability to interact with central nervous system targets. Researchers also investigate its use in creating novel ligands for imaging or diagnostic purposes, leveraging its chemical reactivity and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $89.18 |
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| 1.000 | 10-20 days | $222.33 |
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| 5.000 | 10-20 days | $891.00 |
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(4-(1H-Pyrazol-1-yl)phenyl)methanamine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific receptors or enzymes in therapeutic applications. Its structure, featuring a pyrazole moiety, makes it valuable in designing compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it is explored in the development of small-molecule inhibitors for treating neurological disorders due to its ability to interact with central nervous system targets. Researchers also investigate its use in creating novel ligands for imaging or diagnostic purposes, leveraging its chemical reactivity and stability.
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