2-(4-Chlorophenyl)succinic acid
95%
- Product Code: 86660
CAS:
58755-91-2
| Molecular Weight: | 228.63 g./mol | Molecular Formula: | C₁₀H₉ClO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00598653 | |
| Melting Point: | Boiling Point: | 344.9 °C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily used in the synthesis of various pharmaceutical intermediates. It serves as a key building block in the production of active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting inflammatory and autoimmune conditions. Its structure allows for modifications that enhance biological activity, making it valuable in medicinal chemistry.
Additionally, it is utilized in organic synthesis for the preparation of complex molecules, including polymers and fine chemicals. Its reactive carboxyl groups enable it to participate in condensation and coupling reactions, facilitating the creation of specialized materials.
In research, it is often employed as a reference compound or reagent in studies exploring enzyme inhibition and metabolic pathways. Its stability and well-defined properties make it a reliable choice for experimental applications in biochemistry and pharmacology.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $53.82 |
+
-
|
| 1.000 | 10-20 days | $127.83 |
+
-
|
| 5.000 | 10-20 days | $378.25 |
+
-
|
2-(4-Chlorophenyl)succinic acid
This compound is primarily used in the synthesis of various pharmaceutical intermediates. It serves as a key building block in the production of active pharmaceutical ingredients (APIs), particularly in the development of drugs targeting inflammatory and autoimmune conditions. Its structure allows for modifications that enhance biological activity, making it valuable in medicinal chemistry.
Additionally, it is utilized in organic synthesis for the preparation of complex molecules, including polymers and fine chemicals. Its reactive carboxyl groups enable it to participate in condensation and coupling reactions, facilitating the creation of specialized materials.
In research, it is often employed as a reference compound or reagent in studies exploring enzyme inhibition and metabolic pathways. Its stability and well-defined properties make it a reliable choice for experimental applications in biochemistry and pharmacology.
| 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 :