(3,4-Dimethoxyphenyl)(phenyl)methanone
98%
- Product Code: 85977
CAS:
4038-14-6
| Molecular Weight: | 242.27 g./mol | Molecular Formula: | C₁₅H₁₄O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075875 | |
| Melting Point: | Boiling Point: | 380.7°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is widely used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. Its structure makes it valuable in the development of compounds with potential biological activity, particularly in the field of medicinal chemistry. It is often employed in the synthesis of benzodiazepines and other heterocyclic compounds, which are important in the treatment of anxiety, insomnia, and other neurological disorders. Additionally, it serves as a key building block in the creation of UV absorbers and photoinitiators used in coatings, adhesives, and inks. Its methoxy groups enhance its reactivity, making it a versatile reagent in cross-coupling reactions and other catalytic processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿580.00 |
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| 10.000 | 10-20 days | ฿920.00 |
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| 25.000 | 10-20 days | ฿1,680.00 |
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| 100.000 | 10-20 days | ฿5,250.00 |
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| 500.000 | 10-20 days | ฿18,330.00 |
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(3,4-Dimethoxyphenyl)(phenyl)methanone
This compound is widely used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. Its structure makes it valuable in the development of compounds with potential biological activity, particularly in the field of medicinal chemistry. It is often employed in the synthesis of benzodiazepines and other heterocyclic compounds, which are important in the treatment of anxiety, insomnia, and other neurological disorders. Additionally, it serves as a key building block in the creation of UV absorbers and photoinitiators used in coatings, adhesives, and inks. Its methoxy groups enhance its reactivity, making it a versatile reagent in cross-coupling reactions and other catalytic processes.
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