(R)-3-(Boc-amino)-3-(4-bromophenyl)propionic acid
95%
- Product Code: 104666
CAS:
261380-20-5
| Molecular Weight: | 344.20 g./mol | Molecular Formula: | C₁₄H₁₈BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01320860 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of chiral compounds, which are essential for creating drugs with specific biological activities. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective reactions to be carried out on other parts of the molecule without affecting the amino group. The bromophenyl moiety provides a site for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in drug discovery. Its chiral nature makes it valuable in the synthesis of enantiomerically pure substances, which are crucial for producing medications with higher efficacy and fewer side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,213.00 |
+
-
|
| 1.000 | 10-20 days | ฿9,990.00 |
+
-
|
(R)-3-(Boc-amino)-3-(4-bromophenyl)propionic acid
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of chiral compounds, which are essential for creating drugs with specific biological activities. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective reactions to be carried out on other parts of the molecule without affecting the amino group. The bromophenyl moiety provides a site for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in drug discovery. Its chiral nature makes it valuable in the synthesis of enantiomerically pure substances, which are crucial for producing medications with higher efficacy and fewer side effects.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :