CAS 107890-32-4

1-(4-(Trifluoromethyl)benzyl)piperazine

Description:

1-(4-(Trifluoromethyl)benzyl)piperazine is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The compound features a benzyl group substituted with a trifluoromethyl group at the para position, contributing to its unique properties. The trifluoromethyl group is known for enhancing lipophilicity and influencing the compound's biological activity. This substance is often studied in medicinal chemistry due to its potential pharmacological applications, particularly in the development of psychoactive agents and as a scaffold for various drug candidates. Its molecular structure allows for interactions with various biological targets, making it of interest in research related to neuropharmacology and other therapeutic areas. Additionally, the presence of fluorine atoms can affect the compound's stability and reactivity, which are important considerations in drug design and synthesis. Safety and handling precautions should be observed, as with many chemical substances, due to potential toxicity and environmental impact.

Formula: C₁₂H₁₇F₃N₂

InChI: InChI=1/C12H15F3N2/c13-12(14,15)11-3-1-10(2-4-11)9-17-7-5-16-6-8-17/h1-4,16H,5-9H2/p+2

Synonyms:

• Piperazine, 1-[[4-(Trifluoromethyl)Phenyl]Methyl]-
• 1-[4-(Trifluoromethyl)Benzyl]Piperazinediium
• 1-[4-(Trifluoromethyl)benzyl]piperazine

1-(4-Trifluoromethylbenzyl)piperazine

CAS: 107890-32-4

Formula: C₁₂H₁₅F₃N₂

Purity: >97.0%(GC)(T)

Color and Shape: Light orange to Yellow to Green clear liquid

Molecular weight: 244.26

Ref: 3B-T3075

1-(4-Trifluoromethylbenzyl)piperazine

Controlled Product

CAS: 107890-32-4

Piperazine is a nitrogenous organic compound with a six-membered ring. It has been shown to be an inhibitor of some viruses, including influenza virus, herpes virus, and human immunodeficiency virus type 1 (HIV-1). Piperazine has been shown to inhibit the replication of both RNA and DNA viruses in vitro. This drug also inhibits the replication of hepatitis B virus in vitro and has been shown to have an inhibitory effect on the replication of HIV-1 in vitro. Piperazine is not active against RNA or DNA viruses that use only reverse transcriptase for viral replication. The chemical structure of piperazine is similar to that of amines, which are known to have antiviral properties. Piperazine can be synthesized from benzaldehyde and ammonia by reaction with hydrochloric acid and sodium nitrate.

Formula: C₁₂H₁₅F₃N₂

Purity: Min. 95%

Molecular weight: 244.26 g/mol

Ref: 3D-FT75444