3-Amino-5-(4-fluorophenyl)thiophene-2-carbonitrile is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of an amino group (-NH2) at the 3-position and a cyano group (-C≡N) at the 2-position contributes to its reactivity and potential applications in pharmaceuticals and agrochemicals. The 4-fluorophenyl substituent at the 5-position enhances the compound's electronic properties and may influence its biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential for hydrogen bonding and π-π stacking interactions, which can be relevant in drug design and material science. The CAS number 210356-63-1 uniquely identifies this compound in chemical databases, facilitating its study and application in various fields, including medicinal chemistry and materials science. Overall, the unique combination of functional groups and the thiophene core make it a compound of interest for further research and development.

3-amino-5-(4-fluorophenyl)thiophene-2-carbonitrile

210356-63-1: 3-Amino-5-(4-fluorophenyl)thiophene-2-carbonitrile is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of an amino group (-NH2) at the 3-position and a cyano group (-C≡N) at the 2-position contributes to its reactivity and potential applications in pharmaceuticals and agrochemicals. The 4-fluorophenyl substituent at the 5-position enhances the compound's electronic properties and may influence its biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential for hydrogen bonding and π-π stacking interactions, which can be relevant in drug design and material science. The CAS number 210356-63-1 uniquely identifies this compound in chemical databases, facilitating its study and application in various fields, including medicinal chemistry and materials science. Overall, the unique combination of functional groups and the thiophene core make it a compound of interest for further research and development.

2-Thiophenecarbonitrile, 3-amino-5-(4-fluorophenyl)-

3-Amino-2-cyano-5-(4-fluorophenyl)thiophene

CAS 210356-63-1

3-amino-5-(4-fluorophenyl)thiophene-2-carbonitrile

2-Thiophenecarbonitrile, 3-amino-5-(4-fluorophenyl)-

Ref: IN-DA002KQK

3-Amino-2-cyano-5-(4-fluorophenyl)thiophene

Ref: 54-PC1070Q

3-Amino-2-cyano-5-(4-fluorophenyl)thiophene

Ref: 10-F008187