Ethyl 4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]-3-oxobutanoate CAS:88150-75-8
Name:Ethyl 4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]-3-oxobutanoate CAS:88150-75-8 Synonyms: Amlodipine Process Impurity 1 MF:C16H17NO6 MW:319.31 EINECS:618-122-3 COA:Provide Purity:95%+ Appearance:Yellow oil
Categories:
Material Chemistry
Other Material Chemicals
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Product introduction
| PRODUCT NAME | Ethyl 4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]-3-oxobutanoate |
| CAS NO | 88150-75-8 |
| Synonyms | Amlodipine Process Impurity 1 |
| BP | 479.7±30.0 °C(Predicted) |
| DENSITY | 1.297±0.06 g/cm3(Predicted) |
| STORAGE | 2-8°C |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of Ethyl 4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]-3-oxobutanoate CAS:88150-75-8
Ethyl 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoate, also known as EIOB, is a novel compound that has been studied for its potential applications in scientific research. It is a synthetic compound that belongs to the class of dioxoisoindolin-2-yl compounds and is composed of two parts: ethyl and 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoate. This compound is of interest due to its unique properties and its ability to interact with biological molecules.

Applications of Ethyl 4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]-3-oxobutanoate CAS:88150-75-8
Pharmaceutical Synthesis
N-isoindoline-1,3-dione derivatives have gained significant attention for their potential use in pharmaceutical synthesis . They have shown promising results in the treatment of various diseases and conditions. For instance, some derivatives have been investigated against blood cancer using K562 and Raji cell lines .
Herbicides
These compounds have also found use in the development of herbicides . Their unique chemical structure and reactivity make them suitable for controlling a variety of plant species.
Colorants and Dyes
The isoindoline nucleus and carbonyl groups at positions 1 and 3 give these compounds unique color properties, making them useful in the production of colorants and dyes .
Polymer Additives
N-isoindoline-1,3-dione derivatives can be used as additives in polymers . They can enhance the properties of the polymer, such as its durability, flexibility, and resistance to various environmental factors.
Photochromic Materials
N-isoindoline-1,3-dione derivatives have applications in the development of photochromic materials . These are materials that change color in response to light, and they have a wide range of uses, from eyewear to security inks.
Antiviral Agents
Indole derivatives, which are structurally similar to N-isoindoline-1,3-dione derivatives, have shown potential as antiviral agents . They have been found to inhibit a broad range of RNA and DNA viruses.
Antitubercular Activity
Indole derivatives have also been investigated for their in vitro antitubercular activity . They have shown promising results against Mycobacterium tuberculosis and Mycobacterium bovis.
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