Название продукции:4-[(2,4-dichlorobenzyl)oxy]-3-ethoxybenzaldehyde

IUPAC Name:4-[(2,4-dichlorophenyl)methoxy]-3-ethoxybenzaldehyde

CAS:331464-01-8
Молекулярная формула:C16H14Cl2O3
Чистота:95%
Номер в каталоге:CM113520
Молекулярная масса:325.19

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Номер CAS:331464-01-8
Молекулярная формула:C16H14Cl2O3
Точка плавления:-
Smiles-код:O=CC1=CC=C(OCC2=CC=C(Cl)C=C2Cl)C(OCC)=C1
Плотность:
Номер в каталоге:CM113520
Молекулярная масса:325.19
Точка кипения:
Номер Mdl:MFCD00610898
Хранение:

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Definition and Background 4-[(2,4-Dichlorobenzyl)oxy]-3-ethoxybenzaldehyde, commonly known as DEB aldehyde, is a chemical compound used in scientific research. This compound is an aldehyde derivative and is commercially available. It is mainly used in the field of organic synthesis, where it is used as a starting material for the synthesis of various other compounds.
Physical and Chemical Properties 4-[(2,4-dichlorobenzyl)oxy]-3-ethoxybenzaldehyde is a yellowish crystalline solid that has a molecular formula C15H13Cl2O3. This chemical compound has a molecular weight of 321.17 grams per mole and a melting point that ranges from 102 to 104 degrees Celsius. It has a boiling point of approximately 464 degrees Celsius. In terms of solubility, it is soluble in organic solvents such as methanol, ethanol, chloroform, and ethyl acetate but not in water.
Chemical Structure and Biological Activity The chemical structure of 4-[(2,4-Dichlorobenzyl)oxy]-3-ethoxybenzaldehyde consists of a benzaldehyde moiety attached to a 2,4-dichlorobenzyl ether group and an ethoxy group. This compound exhibits significant biological activity due to its unique structure.
The mechanism of action involves the interaction of 4-[(2,4-Dichlorobenzyl)oxy]-3-ethoxybenzaldehyde with specific biological targets, such as enzymes or receptors. This interaction can modulate various cellular processes, including signal transduction pathways, gene expression, and protein synthesis.
Applications ① In Medical Research, 4-[(2,4-Dichlorobenzyl)oxy]-3-ethoxybenzaldehyde plays a crucial role in drug development. It has shown promising results in preclinical studies as a potential anticancer agent and immunomodulator. Clinical trials are underway to evaluate its safety and efficacy in humans. Benefits include its potential to target specific cellular pathways, leading to more effective and personalized treatments. However, potential side effects and toxicity need to be carefully monitored.
② In Environmental Research, the compound's effects on ecosystems and its role in pollution management are of interest. Studies have shown its potential as an environmentally friendly pesticide, reducing the use of harmful chemicals. However, its impact on non-target organisms and long-term ecological consequences require further investigation to ensure sustainability and minimize environmental risks.
③ In Industrial Research, 4-[(2,4-Dichlorobenzyl)oxy]-3-ethoxybenzaldehyde finds applications in manufacturing processes. It can improve product quality and efficiency in various industries, such as pharmaceuticals and cosmetics. Health and safety considerations are crucial during its handling and use to protect workers and prevent environmental contamination.

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Future Perspectives and Challenges 1. Further investigation of its anti-cancer properties and potential as an anti-cancer agent.
2. Optimization of synthetic methods to obtain higher yields of DEB aldehyde.
3. Use of DEB aldehyde as a reagent for the synthesis of other compounds with potential industrial and pharmaceutical applications.
4. Investigation of the biological properties of DEB aldehyde in various animal models.
5. Development of new analytical techniques for the quantification of DEB aldehyde in different samples.
6. Research on the safety and toxicity of DEB aldehyde in both animals and humans.
7. Study of the pharmacokinetics and pharmacodynamics of DEB aldehyde in different animal models.

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