[2-AMino-5-(Methyloxy)phenyl](4-chlorophenyl)Methanone
98%
- Product Code: 36367
CAS:
91713-54-1
| Molecular Weight: | 261.7 g./mol | Molecular Formula: | C₁₄H₁₂ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20568256 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring both an amino and a methoxy group, makes it a valuable building block for creating compounds with potential biological activity. It is often employed in the synthesis of drug candidates targeting various therapeutic areas, such as central nervous system disorders or inflammatory diseases. Additionally, its chlorophenyl moiety can contribute to the lipophilicity of the resulting molecules, which is crucial for optimizing drug absorption and distribution. Researchers also explore its use in the development of agrochemicals, where its structural features may contribute to the creation of novel pesticides or herbicides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £1,143.15 |
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[2-AMino-5-(Methyloxy)phenyl](4-chlorophenyl)Methanone
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring both an amino and a methoxy group, makes it a valuable building block for creating compounds with potential biological activity. It is often employed in the synthesis of drug candidates targeting various therapeutic areas, such as central nervous system disorders or inflammatory diseases. Additionally, its chlorophenyl moiety can contribute to the lipophilicity of the resulting molecules, which is crucial for optimizing drug absorption and distribution. Researchers also explore its use in the development of agrochemicals, where its structural features may contribute to the creation of novel pesticides or herbicides.
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