| product_name | 2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers |
| CAS_number | Not Available |
| formula | C14H10Cl2FNO3 |
| molar_mass | 346.14 g/mol |
| property_1 | Density: Not Available |
| property_2 | Melting Point: Not Available |
| property_3 | Boiling Point: Not Available |
| property_4 | Solubility: Not Available |
| property_5 | Appearance: Not Available |
| property_6 | Odor: Not Available |
| property_7 | Refractive Index: Not Available |
| property_8 | Flash Point: Not Available |
| property_9 | Stability: Stable under recommended storage conditions |
| property_10 | Storage Conditions: Store in a cool, dry place |
What is the significance of `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers`?
The compound `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers` has shown great potential in various research fields due to its unique chemical structure and properties. It is a key component in the development of innovative drugs and treatments.
How does `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers` work?
This compound works by targeting specific receptors or enzymes in the body, leading to biological effects such as inhibition of certain pathways or modulation of cellular signaling. Its mechanism of action can vary depending on the application and intended use.
What are the potential applications of `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers`?
The compound has shown promise in various applications such as anticancer therapy, anti-inflammatory treatments, and neurodegenerative disorder research. It can also be used in chemical biology studies to understand biological processes at the molecular level.
How is `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers` synthesized?
The compound is typically synthesized through a series of organic reactions involving specific starting materials and reagents. The process requires expertise in organic chemistry and purification techniques to obtain a high-quality product for research purposes.
What are the key advantages of using `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers` in research?
One of the main advantages is the compound's high potency and specificity towards its target, which can lead to more effective results in biological assays or drug screening studies. Additionally, its versatile chemical structure allows for modifications to enhance its properties for different applications.
Are there any limitations or challenges associated with `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers`?
Like any other research compound, there may be challenges related to its stability, solubility, or bioavailability. Researchers should carefully consider these factors when designing experiments or formulating drug formulations using this compound.
What are some recent developments or studies involving `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers`?
Recent studies have highlighted the compound's potential in cancer immunotherapy, where it has been shown to enhance the immune response against tumors. Other research has focused on its neuroprotective effects in neurodegenerative diseases such as Alzheimer's and Parkinson's.
Overall, `2-(2,4-dichloro-5-fluorobenzoyl)-3-cyclopropylaminoacrylic acid, methyl ester, mixture of isomers` presents a valuable tool for researchers and drug developers seeking to advance their understanding of molecular biology and develop novel therapeutics for various diseases. Its unique chemical properties and versatile applications make it a promising candidate for future research and development efforts.