CAS 53065-28-4

6-(phenylsulfanyl)-1H-benzimidazol-2-amine

Description:

6-(Phenylsulfanyl)-1H-benzimidazol-2-amine is a chemical compound characterized by its unique structure, which includes a benzimidazole core substituted with a phenylsulfanyl group and an amino group. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of the benzimidazole moiety, which is known for its role in various pharmacological applications. The phenylsulfanyl group can influence the compound's solubility, stability, and reactivity, making it of interest in medicinal chemistry. Additionally, the presence of the amino group may enhance its ability to form hydrogen bonds, potentially affecting its interaction with biological targets. The compound's molecular weight, melting point, and solubility characteristics would depend on its specific structural features and substituents. Overall, 6-(phenylsulfanyl)-1H-benzimidazol-2-amine represents a class of compounds that may have applications in drug development and other chemical research fields.

Formula: C₁₃H₁₁N₃S

InChI: InChI=1/C13H11N3S/c14-13-15-11-7-6-10(8-12(11)16-13)17-9-4-2-1-3-5-9/h1-8H,(H3,14,15,16)

SMILES: c1ccc(cc1)Sc1ccc2c(c1)[nH]c(=N)[nH]2

Fenbendazole impurity 1

CAS: 53065-28-4

Fenbendazole impurity 1

Color and Shape: Light Brown To Orange

Ref: 47-693

fenbendazoleamine

CAS: 53065-28-4

Formula: C₁₃H₁₁N₃S

Purity: 95%

Color and Shape: Solid

Molecular weight: 241.3115

Ref: IN-DA00DVVH

5-Phenylthio-2-aminobenzimidazole

Controlled Product

CAS: 53065-28-4

Applications 5-Phenylthio-2-aminobenzimidazole, is a derivative of Fenbendazole (F246750), an anthelmintic.
References Baeder, C., et al.: Experientia, 30, 753 (1974), Van der Put, E., et al.: J. Immunol., 173, 818 (2004), Frasca, D., et al.: J. Immunol., 175, 6633 (2005),

Formula: C₁₃H₁₁N₃S

Color and Shape: Light Brown To Orange

Molecular weight: 241.31

Ref: TR-P337725