2-Amino-4-(4-fluorophenyl)thiazole-5-carbonitrile is a heterocyclic organic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features an amino group (-NH2) and a cyano group (-C≡N) attached to the thiazole, contributing to its reactivity and potential biological activity. The presence of a 4-fluorophenyl group enhances its lipophilicity and may influence its interaction with biological targets. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as thiazole derivatives often exhibit various pharmacological properties, including antimicrobial and anticancer activities. The molecular structure allows for various synthetic modifications, which can lead to the development of analogs with improved efficacy or selectivity. Additionally, its unique combination of functional groups may facilitate interactions with specific biological pathways, making it a candidate for further research in therapeutic applications.

2-amino-4-(4-fluorophenyl)thiazole-5-carbonitrile

952753-59-2: 2-Amino-4-(4-fluorophenyl)thiazole-5-carbonitrile is a heterocyclic organic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features an amino group (-NH2) and a cyano group (-C≡N) attached to the thiazole, contributing to its reactivity and potential biological activity. The presence of a 4-fluorophenyl group enhances its lipophilicity and may influence its interaction with biological targets. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as thiazole derivatives often exhibit various pharmacological properties, including antimicrobial and anticancer activities. The molecular structure allows for various synthetic modifications, which can lead to the development of analogs with improved efficacy or selectivity. Additionally, its unique combination of functional groups may facilitate interactions with specific biological pathways, making it a candidate for further research in therapeutic applications.

2-Amino-4-(4-fluorophenyl)-1,3-thiazole-5-carbonitrile

<p>2-Amino-4-(4-fluorophenyl)-1,3-thiazole-5-carbonitrile</p>

CAS 952753-59-2

2-amino-4-(4-fluorophenyl)thiazole-5-carbonitrile

2-Amino-4-(4-fluorophenyl)-1,3-thiazole-5-carbonitrile

Ref: IN-DA00IKND

2-Amino-4-(4-fluorophenyl)-1,3-thiazole-5-carbonitrile

Ref: 54-PC103181

2-Amino-4-(4-fluorophenyl)-1,3-thiazole-5-carbonitrile

Ref: 10-F602701