Methyl (R)-2-(1-aminoethyl)benzoate hcl
95%
- Product Code: 81903
CAS:
1391373-95-7
| Molecular Weight: | 215.68 g./mol | Molecular Formula: | C₁₀H₁₄ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12910776 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a benzoate ester and an amino group, makes it a valuable building block in organic synthesis. It is often employed in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry, ensuring the desired biological activity. Additionally, it serves as a precursor in the creation of compounds with potential therapeutic applications, such as anti-inflammatory or analgesic agents. Its role in asymmetric synthesis is crucial for achieving high enantiomeric purity in drug manufacturing processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $895.03 |
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Methyl (R)-2-(1-aminoethyl)benzoate hcl
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a benzoate ester and an amino group, makes it a valuable building block in organic synthesis. It is often employed in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry, ensuring the desired biological activity. Additionally, it serves as a precursor in the creation of compounds with potential therapeutic applications, such as anti-inflammatory or analgesic agents. Its role in asymmetric synthesis is crucial for achieving high enantiomeric purity in drug manufacturing processes.
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