Introduction to Ethyl Chloro[(4-Methoxyphenyl)Hydrazono]Acetate

CAS: 27143-07-3
Synonyms: Ethyl [(4-methoxyphenyl)hydrazono]chloroacetate, Ethyl (2Z)-chloro[(4-methoxyphenyl)hydrazono]acetate, Ethyl chloro(p-methoxyphenylhydrazono)acetate

Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate is a versatile chemical compound with a wide array of applications in the pharmaceutical and chemical industries. Known for its unique structural features and chemical properties, this compound serves as a building block in the synthesis of novel pharmaceuticals and agrochemicals.

Chemical Properties

Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate showcases remarkable stability and reactivity due to its chloro and hydrazono functional groups. With a molecular formula designed for efficacy, it lends itself to various reactions that facilitate synthetic pathways in drug development.

Molecular Formula: C11H14ClN3O2
Molecular Weight: 257.7 g/mol
Appearance: Pale yellow liquid

Applications

1. Pharmaceuticals:
This compound is extensively utilized in the synthesis of novel hydrazone derivatives, which have demonstrated significant biological activity ranging from antimicrobial to anticancer effects.

2. Agrochemicals:
Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate finds application in developing effective agrochemicals, particularly those aimed at enhancing crop yield and pest resistance.

3. Chemical Research:
As a reagent, this compound plays a crucial role in various synthetic transformations that researchers utilize to explore new pathways and develop innovative chemical entities.

Quality Standards

At Ningbo Inno Pharmchem, we adhere to strict quality control standards to ensure that our Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate meets the high expectations of our customers. We conduct rigorous testing and validation, providing documentation that confirms the purity and quality of our products.

Synthesis Route

Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate can be synthesized via a multi-step reaction involving hydrazine derivatives and ethyl chloroacetate. The method typically involves the following steps:

1. Formation of the Hydrazone:
Hydrolysis and condensation reactions between appropriate hydrazine and an aldehyde or keto compound.

2. Chlorination:
Introducing the chloroacetyl group through standard chlorination methods, ensuring to maintain the structural integrity of the hydrazone.

3. Purification:
The final product is purified using distillation or recrystallization techniques to achieve the desired level of purity.

Conclusion

Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate is a powerful compound with diverse applications in pharmaceutical synthesis, agrochemical development, and chemical research. With exceptional stability and reactivity, it acts as a crucial intermediate in the creation of innovative chemical solutions. Trust Ningbo Inno Pharmchem as your reliable supplier for this unique compound, ensuring high-quality standards and effective performance in your applications.

Discover the potential of Ethyl chloro[(4-methoxyphenyl)hydrazono]acetate and enhance your product development today!

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