2-(2-(Benzyloxy)-4-fluorophenyl)acetonitrile
97%
- Product Code: 81251
CAS:
1824265-83-9
| Molecular Weight: | 241.26 g./mol | Molecular Formula: | C₁₅H₁₂FNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18204938 | |
| Melting Point: | Boiling Point: | 368.1±32.0 °C at 760 mmHg | |
| Density: | 1.2±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical intermediates. It serves as a key building block in the preparation of complex molecules, often contributing to the synthesis of biologically active compounds. Its structure, featuring a benzyloxy group and a fluorophenyl moiety, makes it valuable in the design of potential drug candidates, especially in the field of medicinal chemistry. Researchers leverage its reactivity to introduce specific functional groups or modify existing structures, aiding in the creation of compounds with targeted therapeutic properties. Additionally, it may be employed in the study of chemical reactions involving nitrile groups, providing insights into reaction mechanisms and pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,900.00 |
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| 1.000 | 10-20 days | ฿27,000.00 |
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2-(2-(Benzyloxy)-4-fluorophenyl)acetonitrile
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical intermediates. It serves as a key building block in the preparation of complex molecules, often contributing to the synthesis of biologically active compounds. Its structure, featuring a benzyloxy group and a fluorophenyl moiety, makes it valuable in the design of potential drug candidates, especially in the field of medicinal chemistry. Researchers leverage its reactivity to introduce specific functional groups or modify existing structures, aiding in the creation of compounds with targeted therapeutic properties. Additionally, it may be employed in the study of chemical reactions involving nitrile groups, providing insights into reaction mechanisms and pathways.
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