(4S,5R)-4-(Fluoromethyl)-5-(4-iodophenyl)-2-phenyl-4,5-dihydrooxazole
97%
- Product Code: 70931
CAS:
927689-69-8
| Molecular Weight: | 381.18 g./mol | Molecular Formula: | C₁₆H₁₃FINO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27977270 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of complex pharmaceutical agents. Its unique structure, featuring both fluoromethyl and iodophenyl groups, makes it particularly valuable in the development of targeted drug molecules. Researchers often employ it in the creation of potential therapeutic compounds, especially those aimed at treating neurological disorders or cancers. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, enabling the attachment of various bioactive moieties. Additionally, its oxazole ring contributes to the stability and bioavailability of the resulting drug candidates. This chemical is also explored in radiopharmaceuticals, where the iodine isotope can be used for imaging or therapeutic purposes. Its applications extend to organic synthesis, where it serves as a versatile building block for constructing more complex molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,556.00 |
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| 0.250 | 10-20 days | ฿5,112.00 |
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(4S,5R)-4-(Fluoromethyl)-5-(4-iodophenyl)-2-phenyl-4,5-dihydrooxazole
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of complex pharmaceutical agents. Its unique structure, featuring both fluoromethyl and iodophenyl groups, makes it particularly valuable in the development of targeted drug molecules. Researchers often employ it in the creation of potential therapeutic compounds, especially those aimed at treating neurological disorders or cancers. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, enabling the attachment of various bioactive moieties. Additionally, its oxazole ring contributes to the stability and bioavailability of the resulting drug candidates. This chemical is also explored in radiopharmaceuticals, where the iodine isotope can be used for imaging or therapeutic purposes. Its applications extend to organic synthesis, where it serves as a versatile building block for constructing more complex molecular architectures.
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