3-Amino-[1,1'-biphenyl]-4-carboxylic acid
97%
- Product Code: 117816
CAS:
4445-43-6
| Molecular Weight: | 213.23 g./mol | Molecular Formula: | C₁₃H₁₁NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00577380 | |
| Melting Point: | Boiling Point: | 427°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals and organic materials. It serves as a key intermediate in the production of various drugs, particularly those targeting inflammation and cancer. Its biphenyl structure allows it to act as a building block for creating complex molecules with specific biological activities. Additionally, it is used in the development of fluorescent dyes and sensors due to its aromatic properties, which enhance light absorption and emission. In research, it is employed to study molecular interactions and design new compounds with potential therapeutic applications. Its carboxylic acid group also makes it suitable for coupling reactions, further expanding its utility in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,836.00 |
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| 0.250 | 10-20 days | ฿3,672.00 |
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3-Amino-[1,1'-biphenyl]-4-carboxylic acid
This compound is primarily utilized in the synthesis of pharmaceuticals and organic materials. It serves as a key intermediate in the production of various drugs, particularly those targeting inflammation and cancer. Its biphenyl structure allows it to act as a building block for creating complex molecules with specific biological activities. Additionally, it is used in the development of fluorescent dyes and sensors due to its aromatic properties, which enhance light absorption and emission. In research, it is employed to study molecular interactions and design new compounds with potential therapeutic applications. Its carboxylic acid group also makes it suitable for coupling reactions, further expanding its utility in organic synthesis.
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