| product_name | 3-Chlorocarbonylacrylic acid ethyl ester |
| CAS_number | 6236-88-4 |
| formula | C6H7ClO3 |
| molar_mass | 162.57 |
| boiling_point | None available |
| melting_point | None available |
| density | None available |
| appearance | None available |
| pH | None available |
| solubility_in_water | None available |
| vapor_pressure | None available |
| flash_point | None available |
| autoignition_temperature | None available |
| stability | Stable under recommended storage conditions |
| storage_conditions | Store in a cool, dry, and well-ventilated place |
What is 3-Chlorocarbonylacrylic acid ethyl ester?
3-Chlorocarbonylacrylic acid ethyl
ester is a chemical compound that is commonly used in organic synthesis and research labs.
It is an ester of acrylic acid that contains a chlorine atom on the alpha carbon.
How
is 3-Chlorocarbonylacrylic acid ethyl ester used in organic
synthesis?
3-Chlorocarbonylacrylic acid ethyl ester is often used as a reagent in
organic synthesis reactions due to its ability to form a variety of functionalized products.
It can undergo nucleophilic addition, acylation, and other types of reactions to introduce
different functional groups into a molecule.
What are some common reactions that can
be carried out using 3-Chlorocarbonylacrylic acid ethyl ester?
Some common reactions
that can be carried out using 3-Chlorocarbonylacrylic acid ethyl ester include Wittig
reactions, Michael additions, and Knoevenagel condensations. These reactions allow for the
formation of carbon-carbon and carbon-oxygen bonds, among others.
What are the
benefits of using 3-Chlorocarbonylacrylic acid ethyl ester in
research?
3-Chlorocarbonylacrylic acid ethyl ester is a versatile compound that can
be used to synthesize a wide range of organic molecules. Its unique structure and reactivity
make it a valuable tool for researchers looking to create complex chemical
structures.
Are there any safety considerations to keep in mind when working with
3-Chlorocarbonylacrylic acid ethyl ester?
As with any chemical compound, it is
important to follow proper safety procedures when handling 3-Chlorocarbonylacrylic acid
ethyl ester. This includes wearing appropriate personal protective equipment, working in a
well-ventilated area, and following all recommended storage and handling
guidelines.
Can 3-Chlorocarbonylacrylic acid ethyl ester be used in pharmaceutical
research?
Yes, 3-Chlorocarbonylacrylic acid ethyl ester can be used in pharmaceutical
research as a building block for the synthesis of bioactive compounds. Its reactivity and
ability to introduce functional groups make it a valuable tool for drug discovery and
development.
What are some examples of compounds that can be synthesized using
3-Chlorocarbonylacrylic acid ethyl ester?
Compounds such as acyl chlorides, esters,
and amides can be synthesized using 3-Chlorocarbonylacrylic acid ethyl ester as a starting
material. These compounds can then be further modified to create more complex molecules for
various applications.
Are there any alternative methods for synthesizing compounds
similar to 3-Chlorocarbonylacrylic acid ethyl ester?
While there are alternative
methods for synthesizing similar compounds, 3-Chlorocarbonylacrylic acid ethyl ester offers
advantages such as ease of use, high purity, and good yields in many reactions. Researchers
may choose to use this compound based on these factors and its compatibility with a wide
range of organic reactions.
In conclusion, 3-Chlorocarbonylacrylic acid ethyl ester
is a valuable compound for organic synthesis and research due to its reactivity,
versatility, and ability to produce a variety of functionalized products. Researchers in
various fields can utilize this compound to create complex molecules and advance their
research goals.
