2-Thiophen-3-ylethanamine, with the CAS number 59311-67-0, is an organic compound characterized by the presence of a thiophene ring and an ethylamine functional group. The thiophene moiety contributes to its aromatic properties, while the ethylamine part introduces basic characteristics due to the amine group. This compound typically exhibits a pale yellow to brownish color and is soluble in polar organic solvents. Its structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry and drug development. The presence of the thiophene ring can enhance its ability to interact with various biological targets, potentially influencing its pharmacological properties. Additionally, 2-thiophen-3-ylethanamine may participate in various chemical reactions, including alkylation and acylation, due to the reactivity of the amine group. Overall, this compound's unique structural features and functional groups make it a subject of interest in both synthetic and applied chemistry.

2-thiophen-3-ylethanamine

59311-67-0: 2-(3-Thienyl)Ethanamine, 2-(Thiophen-3-Yl)Ethan-1-Amine, 3-Thiopheneethanamine

2-(3-Thienyl)ethanamine

2-(3-Thienyl)ethanamine is a fluorescent compound that has been shown to be an acceptor for fluorescence resonance energy transfer. It also has the ability to form a conformational equilibrium between two different tautomers, which can be distinguished by their nmr spectra. 2-(3-Thienyl)ethanamine is an enzyme inhibitor that blocks the conversion of polyphosphoric acid into polyphosphate by inhibiting the enzyme polyphosphate kinase. The synthesis of this compound involves reacting 3-phenylacetonitrile with ethylamine and triethyloxonium chloride. This synthetic process produces substituted amines and alkylating agents as side products.

CAS 59311-67-0: 2-thiophen-3-ylethanamine

2-(3-Thienyl)ethanamine

Ref: 10-F219002

2-(3-Thienyl)ethanamine

Ref: 3D-JCA31167

2-(3-THIENYL)ETHANAMINE

Ref: IN-DA00E9P1

2-(Thiophen-3-yl)ethan-1-amine

Ref: 54-OR1021114