N-Methyl-N-propargylbenzylamine
≥98%
- Product Code: 67660
CAS:
555-57-7
| Molecular Weight: | 159.23 g./mol | Molecular Formula: | C₁₁H₁₃N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00008576 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
N-Methyl-N-propargylbenzylamine is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of molecules with potential neuroprotective properties. The propargyl group in its structure makes it a valuable precursor in click chemistry reactions, enabling the formation of triazole derivatives, which are significant in drug discovery and material science. Additionally, it is used in the preparation of bioactive molecules targeting neurological disorders, such as Parkinson’s disease, due to its ability to modulate monoamine oxidase activity. Its benzylamine moiety also contributes to its role in the synthesis of ligands for various receptors, aiding in the study of biochemical pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Light yellow to Light orange clear liquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿950.00 |
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| 1.000 | 10-20 days | ฿1,990.00 |
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N-Methyl-N-propargylbenzylamine
N-Methyl-N-propargylbenzylamine is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of molecules with potential neuroprotective properties. The propargyl group in its structure makes it a valuable precursor in click chemistry reactions, enabling the formation of triazole derivatives, which are significant in drug discovery and material science. Additionally, it is used in the preparation of bioactive molecules targeting neurological disorders, such as Parkinson’s disease, due to its ability to modulate monoamine oxidase activity. Its benzylamine moiety also contributes to its role in the synthesis of ligands for various receptors, aiding in the study of biochemical pathways.
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