N-(2,2-dimethoxy-ethyl)-3,4-dimethoxyphenylacetamide
95%
- Product Code: 50632
CAS:
73954-34-4
| Molecular Weight: | 283.32 g./mol | Molecular Formula: | C₁₄H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30534182 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research. It serves as a key intermediate in the development of bioactive molecules, including potential drugs targeting neurological disorders. Its structure, featuring dimethoxy groups, makes it suitable for reactions requiring specific electron-donating properties, aiding in the creation of compounds with enhanced binding affinity to biological targets. Additionally, it is employed in the study of metabolic pathways and enzyme interactions, contributing to advancements in medicinal chemistry and drug design.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €290.20 |
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| 1.000 | 10-20 days | €1,134.16 |
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N-(2,2-dimethoxy-ethyl)-3,4-dimethoxyphenylacetamide
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research. It serves as a key intermediate in the development of bioactive molecules, including potential drugs targeting neurological disorders. Its structure, featuring dimethoxy groups, makes it suitable for reactions requiring specific electron-donating properties, aiding in the creation of compounds with enhanced binding affinity to biological targets. Additionally, it is employed in the study of metabolic pathways and enzyme interactions, contributing to advancements in medicinal chemistry and drug design.
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