3-Amino-5-(3-fluorophenyl)thiophene-2-carboxylic acid
95%
- Product Code: 44923
CAS:
1184917-64-3
| Molecular Weight: | 237.25 g./mol | Molecular Formula: | C₁₁H₈FNO₂S |
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| EC Number: | MDL Number: | MFCD12405898 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both a thiophene ring and a fluorophenyl group, makes it a valuable intermediate in the creation of biologically active molecules. It is often employed in the design of compounds targeting specific enzymes or receptors, especially in the fields of oncology and neurology. Additionally, its carboxylic acid group allows for further functionalization, enabling the development of more complex molecules with potential therapeutic applications. Researchers also explore its use in the synthesis of fluorescent probes or imaging agents due to its aromatic and heterocyclic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,911.00 |
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| 0.250 | 10-20 days | ฿15,822.00 |
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3-Amino-5-(3-fluorophenyl)thiophene-2-carboxylic acid
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both a thiophene ring and a fluorophenyl group, makes it a valuable intermediate in the creation of biologically active molecules. It is often employed in the design of compounds targeting specific enzymes or receptors, especially in the fields of oncology and neurology. Additionally, its carboxylic acid group allows for further functionalization, enabling the development of more complex molecules with potential therapeutic applications. Researchers also explore its use in the synthesis of fluorescent probes or imaging agents due to its aromatic and heterocyclic properties.
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