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27143-07-3

Acetic acid, chloro[(4-methoxyphenyl)hydrazono]-, ethyl ester

Catalog#: AR00I5UB  |   CAS#: 27143-07-3  |   MDL#: MFCD02852962  |   MF: C11H13ClN2O3  |   MW: 256.6855

Packsize Purity Price Availability Quantity
1g 97% $4.00 Global Stock Buy Now Add To Cart
5g 97% $18.00 Global Stock Buy Now Add To Cart
10g 97% $32.00 Global Stock Buy Now Add To Cart
25g 97% $61.00 Global Stock Buy Now Add To Cart
100g 97% $174.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00I5UB
Chemical Name Acetic acid, chloro[(4-methoxyphenyl)hydrazono]-, ethyl ester
CAS Number 27143-07-3
Molecular Formula C11H13ClN2O3
Molecular Weight 256.6855
MDL Number MFCD02852962
SMILES CCOC(=O)/C(=N/Nc1ccc(cc1)OC)/Cl

Ethyl 2-chloro-2-(2-(4-methoxyphenyl)hydrazono)acetate is a versatile compound that finds extensive application in chemical synthesis due to its unique reactivity and functional groups. This compound serves as an important building block in organic chemistry, enabling the synthesis of various complex molecules through diverse reactions.The presence of the chloro and hydrazono functional groups in Ethyl 2-chloro-2-(2-(4-methoxyphenyl)hydrazono)acetate makes it a valuable reagent for nucleophilic substitution reactions. These reactions involve the displacement of the chlorine atom by a nucleophile, leading to the formation of new carbon-nitrogen or carbon-oxygen bonds. This capability allows for the introduction of diverse functional groups into the molecule, facilitating the synthesis of structurally diverse compounds.Furthermore, the presence of the methoxyphenyl group in Ethyl 2-chloro-2-(2-(4-methoxyphenyl)hydrazono)acetate imparts aromatic properties to the molecule, making it suitable for reactions involving aromatic systems. The methoxy group can participate in various aromatic substitution reactions, expanding the range of transformations that can be carried out using this compound in chemical synthesis.Overall, Ethyl 2-chloro-2-(2-(4-methoxyphenyl)hydrazono)acetate is a valuable tool in the hands of synthetic chemists, offering a versatile platform for the construction of complex organic molecules through strategic manipulations of its functional groups. Its unique reactivity and functional diversity make it an indispensable component in the toolbox of organic chemists striving to create novel compounds for various applications.
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