(E)-5-(3-Aminophenyl)-2-penten-4-ynoic Acid Ethyl Ester Trifluoroacetic Acid Salt, with CAS number 1346606-68-5, is a chemical compound characterized by its unique structural features, including an ethyl ester functional group and a trifluoroacetic acid salt formation. This compound typically exhibits properties associated with both organic acids and amines, such as solubility in polar solvents and potential reactivity due to the presence of the alkyne and amine functionalities. The (E) configuration indicates a specific geometric arrangement around the double bond, which can influence its biological activity and interaction with other molecules. The trifluoroacetic acid component enhances the compound's stability and solubility in various solvents, making it useful in synthetic chemistry and pharmaceutical applications. Additionally, the presence of the amino group suggests potential for hydrogen bonding and interaction with biological targets, which may be relevant in medicinal chemistry. Overall, this compound's characteristics make it a subject of interest in research and development within the fields of organic synthesis and drug design.

(E)-5-(3-AMinophenyl)-2-penten-4-ynoic Acid Ethyl Ester Trifluoroacetic Acid Salt

1346606-68-5: (E)-5-(3-Aminophenyl)-2-penten-4-ynoic Acid Ethyl Ester Trifluoroacetic Acid Salt, with CAS number 1346606-68-5, is a chemical compound characterized by its unique structural features, including an ethyl ester functional group and a trifluoroacetic acid salt formation. This compound typically exhibits properties associated with both organic acids and amines, such as solubility in polar solvents and potential reactivity due to the presence of the alkyne and amine functionalities. The (E) configuration indicates a specific geometric arrangement around the double bond, which can influence its biological activity and interaction with other molecules. The trifluoroacetic acid component enhances the compound's stability and solubility in various solvents, making it useful in synthetic chemistry and pharmaceutical applications. Additionally, the presence of the amino group suggests potential for hydrogen bonding and interaction with biological targets, which may be relevant in medicinal chemistry. Overall, this compound's characteristics make it a subject of interest in research and development within the fields of organic synthesis and drug design.

<p>Applications Intermediate in the synthesis of Oxamflatin (O845090)<br></p>

CAS 1346606-68-5

(E)-5-(3-AMinophenyl)-2-penten-4-ynoic Acid Ethyl Ester Trifluoroacetic Acid Salt

(E)-5-(3-Aminophenyl)-2-penten-4-ynoic Acid Ethyl Ester Trifluoroacetic Acid Salt

Ref: TR-A625800