| 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.
