methyl 2-amino-2-(4-bromophenyl)-4-methylpentanoate
- Product Code: 77125
CAS:
1523617-93-7
| Molecular Weight: | 300.19 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26404035 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both an amino group and a bromophenyl moiety, makes it a versatile building block for constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) that target neurological disorders, due to its potential to interact with specific receptors in the brain. Additionally, its ester group allows for further chemical modifications, enabling the creation of derivatives with tailored properties for medicinal chemistry research. The bromine atom in its structure also facilitates coupling reactions, making it valuable in cross-coupling processes used to develop novel drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿388,080.00 |
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methyl 2-amino-2-(4-bromophenyl)-4-methylpentanoate
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both an amino group and a bromophenyl moiety, makes it a versatile building block for constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) that target neurological disorders, due to its potential to interact with specific receptors in the brain. Additionally, its ester group allows for further chemical modifications, enabling the creation of derivatives with tailored properties for medicinal chemistry research. The bromine atom in its structure also facilitates coupling reactions, making it valuable in cross-coupling processes used to develop novel drug candidates.
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