Methyl 3-(4-chlorophenyl)-3-oxopropanoate
97%
- Product Code: 83529
CAS:
22027-53-8
| Molecular Weight: | 212.63 g./mol | Molecular Formula: | CH₉ClO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00216520 | |
| Melting Point: | 42-46 °C(lit.) | Boiling Point: | 298.9 °C at 760 mmHg |
| Density: | 1.255 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a 4-chlorophenyl group and a keto ester functionality, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the preparation of compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or antifungal agents. Additionally, it serves as a precursor in the development of fine chemicals and specialty materials, where its reactive sites enable further functionalization and modification. Its applications also extend to research settings, where it is used in the study of reaction mechanisms and the development of novel synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,151.00 |
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Methyl 3-(4-chlorophenyl)-3-oxopropanoate
This compound is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a 4-chlorophenyl group and a keto ester functionality, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the preparation of compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or antifungal agents. Additionally, it serves as a precursor in the development of fine chemicals and specialty materials, where its reactive sites enable further functionalization and modification. Its applications also extend to research settings, where it is used in the study of reaction mechanisms and the development of novel synthetic methodologies.
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