CAS 72490-14-3

Ethanamine, 2-(4-phenoxyphenoxy)-

Description:

Ethanamine, 2-(4-phenoxyphenoxy)-, also known by its CAS number 72490-14-3, is an organic compound characterized by the presence of an ethanamine backbone with a phenoxyphenyl substituent. This compound features an amine functional group (-NH2) attached to a two-carbon ethyl chain, which is further substituted with a phenoxy group, indicating the presence of an ether linkage between a phenyl ring and an oxygen atom. The structure suggests potential applications in pharmaceuticals or as a chemical intermediate due to its ability to participate in various chemical reactions, including nucleophilic substitutions. The presence of aromatic rings in its structure may contribute to its stability and influence its solubility and reactivity. Additionally, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization. Safety data should also be consulted to understand any hazards associated with handling this substance.

Formula: C₁₄H₁₅NO₂

Ethanamine, 2-(4-phenoxyphenoxy)-

CAS: 72490-14-3

Formula: C₁₄H₁₅NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 229.2744

Ref: IN-DA0065SU

2-(4-Phenoxyphenoxy)ethanamine

Controlled Product

CAS: 72490-14-3

Applications 2-(4-Phenoxyphenoxy)ethanamine is an intermediate in the synthesis of Fenoxycarb-d3 (F248871), a labelled form of Fenoxycarb (F248870). Fenoxycarb is a carbamate insect growth regulator by preventing immature insects from reaching maturity by mimicking juvenile hormone. Used as a standard for Pesticide detection. Fenoxycarb is also used in cannabis testing kits as a component of pesticide mixes (P698235).
References El-Saeid, M.H., et al.: J. Chem., 10, (2013); Coors, A., et al.: Environ. Toxicol. Chem., 31, 1239 (2012);

Formula: C₁₄H₁₅NO₂

Color and Shape: Neat

Molecular weight: 229.27

Ref: TR-P318675