4-(Dimethylamino)but-2-enoic acid hydrochloride
98% (only trans)
- Product Code: 46461
CAS:
98548-81-3
| Molecular Weight: | 165.62 g./mol | Molecular Formula: | C₆H₁₂ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of drugs that target the central nervous system. Its structure, featuring both a dimethylamino group and a carboxylic acid, makes it versatile for modifications and reactions, enabling the creation of compounds with potential therapeutic properties. Additionally, it is employed in research settings to study reaction mechanisms and develop new synthetic methodologies. Its hydrochloride form enhances stability and solubility, making it easier to handle in various chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿760.00 |
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| 5.000 | 10-20 days | ฿2,790.00 |
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| 10.000 | 10-20 days | ฿5,270.00 |
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4-(Dimethylamino)but-2-enoic acid hydrochloride
This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of drugs that target the central nervous system. Its structure, featuring both a dimethylamino group and a carboxylic acid, makes it versatile for modifications and reactions, enabling the creation of compounds with potential therapeutic properties. Additionally, it is employed in research settings to study reaction mechanisms and develop new synthetic methodologies. Its hydrochloride form enhances stability and solubility, making it easier to handle in various chemical processes.
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