Bis(4-methoxybenzyl)amine hydrochloride
97%
- Product Code: 72982
CAS:
854391-95-0
| Molecular Weight: | 293.79 g./mol | Molecular Formula: | C₁₆H₂₀ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 243-245°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Bis(4-methoxybenzyl)amine hydrochloride is primarily used in organic synthesis as a building block for the preparation of more complex chemical compounds. It serves as an intermediate in the development of pharmaceutical agents, particularly in the synthesis of compounds with potential therapeutic applications. Its structure, featuring methoxybenzyl groups, makes it valuable in the creation of molecules with specific biological activities, such as receptor antagonists or enzyme inhibitors. Additionally, it is utilized in research settings for the study of chemical reactions and the development of new synthetic methodologies. Its stability and reactivity under various conditions make it a versatile reagent in medicinal chemistry and drug discovery processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | SOLID |
| PURITY | 96.5 |
| MELTING POINT | 235-250 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $15.07 |
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| 1.000 | 10-20 days | $25.62 |
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| 5.000 | 10-20 days | $89.40 |
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| 25.000 | 10-20 days | $309.39 |
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Bis(4-methoxybenzyl)amine hydrochloride
Bis(4-methoxybenzyl)amine hydrochloride is primarily used in organic synthesis as a building block for the preparation of more complex chemical compounds. It serves as an intermediate in the development of pharmaceutical agents, particularly in the synthesis of compounds with potential therapeutic applications. Its structure, featuring methoxybenzyl groups, makes it valuable in the creation of molecules with specific biological activities, such as receptor antagonists or enzyme inhibitors. Additionally, it is utilized in research settings for the study of chemical reactions and the development of new synthetic methodologies. Its stability and reactivity under various conditions make it a versatile reagent in medicinal chemistry and drug discovery processes.
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