(S,E)-Methyl 2-amino-4-(4-(trifluoromethyl)phenyl)but-3-enoate hydrochloride
97%
- Product Code: 38649
CAS:
2098497-09-5
| Molecular Weight: | 295.69 g./mol | Molecular Formula: | C₁₂H₁₃ClF₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22573747 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its structure, featuring a trifluoromethyl group and an amino ester moiety, makes it a valuable intermediate in the creation of potential drug candidates. It is often employed in the design of compounds targeting specific enzymes or receptors, especially in areas like anti-inflammatory, anticancer, or central nervous system therapies. The trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting molecules, while the amino ester functionality allows for further chemical modifications. Researchers also use it in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug-like properties. Additionally, it may find application in the development of agrochemicals or other specialty chemicals due to its unique structural features.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿19,395.00 |
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| 0.250 | 10-20 days | ฿38,790.00 |
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(S,E)-Methyl 2-amino-4-(4-(trifluoromethyl)phenyl)but-3-enoate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its structure, featuring a trifluoromethyl group and an amino ester moiety, makes it a valuable intermediate in the creation of potential drug candidates. It is often employed in the design of compounds targeting specific enzymes or receptors, especially in areas like anti-inflammatory, anticancer, or central nervous system therapies. The trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting molecules, while the amino ester functionality allows for further chemical modifications. Researchers also use it in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug-like properties. Additionally, it may find application in the development of agrochemicals or other specialty chemicals due to its unique structural features.
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