Product Introduction
|
CAS Number |
579510-89-7 |
|
Purity |
≥99% |
|
Total impurity |
≤2% |
|
Single impurity |
≤0.5% |
|
Molecular Formula |
C15H12O4 |
|
Molecular Weight |
256.25 |
|
Retest period |
12 months |
|
Storage Condition |
2-8°C |
|
COA/ROS/MSDS/MOA |
Provided |
Application
1. Hydroxylation reaction: 4-Methoxycarbonyl-11-biphenyl-3-carboxylic acid with hydroxyl and ester functional groups can undergo hydroxylation reaction under appropriate conditions to produce hydroxylated products such as 4-hydroxycarbonyl-11-biphenyl-3-carboxylic acid. This reaction can be achieved by acid catalysis or base catalysis.
2. Photocontrolled hydrolysis ability: 4-Methoxycarbonyl-11-biphenyl-3-carboxylic acid is photosensitive, and when irradiated by light of specific wavelength, the ester bond will undergo photocontrolled hydrolysis reaction, thus releasing the carboxylic acid functional group. This photocontrolled hydrolysis ability is widely used in materials science, drug delivery and other fields.
3. Optical materials: 4-Methoxycarbonyl-11-biphenyl-3-carboxylic acid and its derivatives are excellent liquid crystal molecules that can be used to prepare liquid crystal materials. Their liquid crystal material properties can be adjusted by chemical modifications.
4. Pharmaceutical research: 4-Methoxycarbonyl-11-biphenyl-3-carboxylic acid and its derivatives have various biological activities, such as anticancer and antiviral. These compounds have been widely used in the field of pharmaceutical research. For example, 4-methoxycarbonyl-11-biphenyl-3-carboxylic acid analogs can be used as potential oncological therapeutic agents.
Partner
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