CAS 95777-69-8

N-{2-amino-6-[(4-fluorobenzyl)amino]pyridin-3-yl}acetamide hydrochloride (1:1)

Description:

N-{2-amino-6-[(4-fluorobenzyl)amino]pyridin-3-yl}acetamide hydrochloride is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with amino and acetamide functional groups. This compound features a 4-fluorobenzyl group, contributing to its unique properties and potential biological activity. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in pharmaceutical applications. The presence of the amino groups suggests potential for hydrogen bonding, which may influence its interaction with biological targets. This compound may exhibit various pharmacological activities, making it of interest in medicinal chemistry. Its CAS number, 95777-69-8, allows for precise identification and retrieval of information regarding its properties, synthesis, and applications in scientific literature. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function, highlighting its relevance in drug development and research.

Formula: C₁₄H₁₆ClFN₄O

InChI: InChI=1/C14H15FN4O.ClH/c1-9(20)18-12-6-7-13(19-14(12)16)17-8-10-2-4-11(15)5-3-10;/h2-7H,8H2,1H3,(H,18,20)(H3,16,17,19);1H

SMILES: CC(=Nc1ccc(=NCc2ccc(cc2)F)[nH]c1N)O.Cl

D 13223 (Flupirtine Metabolite)

CAS: 95777-69-8

Formula: C₁₄H₁₆ClFN₄O

Purity: 98%

Color and Shape: Solid

Molecular weight: 310.7544

Ref: IN-DA005XDV

D 13223 (Flupirtine Metabolite)

Controlled Product

CAS: 95777-69-8

Applications The major active metabolite of Flupirtine in human plasma. A potassium channel opener
References Niebch, G., et al.: Arzneim.-Forsch., 42, 1343 (1992), Friedel, H., et al.: Drugs, 45, 548 (1993), Fu, I., et al.: J. Pharm. Biomed. Anal., 18, 347 (1998),

Formula: C₁₄H₁₆ClFN₄O

Color and Shape: Neat

Molecular weight: 310.75

Ref: TR-D100065