CAS 350997-18-1

ethyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate

Description:

Ethyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate is an organic compound characterized by its complex structure, which includes a thiophene ring, an amino group, and an ethyl ester functional group. This compound features a naphthalene moiety, contributing to its aromatic characteristics and potential for π-π stacking interactions. The presence of the amino group suggests potential for hydrogen bonding, which may influence its solubility and reactivity. The ethyl ester group enhances its lipophilicity, making it more soluble in organic solvents. This compound may exhibit biological activity, potentially serving as a scaffold for drug development or as a precursor in synthetic organic chemistry. Its unique structure allows for various chemical modifications, which can be explored for applications in pharmaceuticals or materials science. As with many thiophene derivatives, it may also display interesting electronic properties, making it a candidate for use in organic electronics or as a dye. Overall, ethyl 2-amino-4-(naphthalen-1-yl)thiophene-3-carboxylate is a versatile compound with potential applications across multiple fields.

Formula: C₁₇H₁₅NO₂S

InChI: InChI=1/C17H15NO2S/c1-2-20-17(19)15-14(10-21-16(15)18)13-9-5-7-11-6-3-4-8-12(11)13/h3-10H,2,18H2,1H3

SMILES: CCOC(=O)c1c(csc1N)c1cccc2ccccc12

Synonyms:

• 3-Thiophenecarboxylic Acid, 2-Amino-4-(1-Naphthalenyl)-, Ethyl Ester
• Ethyl 2-amino-4-(1-naphthyl)thiophene-3-carboxylate

Ethyl 2-amino-4-(1-naphthyl)thiophene-3-carboxylate

CAS: 350997-18-1

Purity: 95.0%

Molecular weight: 297.3699951171875

Ref: 10-F307168