CAS 103596-43-6

4-fluorodeprenyl

Description:

4-Fluorodeprenyl, with the CAS number 103596-43-6, is a chemical compound that belongs to the class of substituted phenethylamines. It is characterized by the presence of a fluorine atom at the para position of the phenyl ring, which can influence its biological activity and pharmacological properties. This compound is structurally related to deprenyl (selegiline), a well-known monoamine oxidase inhibitor used in the treatment of Parkinson's disease and depression. The introduction of the fluorine atom may enhance its lipophilicity and alter its interaction with biological targets. 4-Fluorodeprenyl is of interest in medicinal chemistry for its potential neuroprotective effects and its role in modulating neurotransmitter levels. Additionally, its synthesis and characterization involve standard organic chemistry techniques, and it may be studied for its effects on the central nervous system. As with many fluorinated compounds, it may exhibit unique reactivity and stability profiles, making it a subject of interest in both pharmaceutical research and chemical synthesis.

Formula: C₁₃H₁₆FN

InChI: InChI=1/C13H16FN/c1-4-9-15(3)11(2)10-12-5-7-13(14)8-6-12/h1,5-8,11H,9-10H2,2-3H3

SMILES: C#CCN(C)C(C)Cc1ccc(cc1)F

Synonyms:

• (R)-(-)-4-Fluorodeprenyl
• (S)-(+)-4-Fluorodeprenyl
• Benzeneethanamine, 4-fluoro-N,alpha-dimethyl-N-2-propynyl-
• N-[1-(4-fluorophenyl)propan-2-yl]-N-methylprop-2-yn-1-amine
• 4-Fluorodeprenyl

N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine

Controlled Product

CAS: 103596-43-6

N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine is a synthetic molecule that has been shown to be an inhibitor of the enzyme nitroethane reductase. This drug is also capable of inhibiting the activity of other enzymes and is being investigated for its potential use in the treatment of various types of cancer. N-[1-(4-Fluorophenyl)propan-2-Yl]-N-methylprop-2-Yn-1-amine inhibits nitroethane reductase by binding reversibly to the active site and competitively inhibiting the substrate. The potency of this drug against nitroethane reductase has been shown to be increased by alkylation.br>
The inhibition of nitroethane reductase by N-[1-(4-fluorophenyl)propan-2-Yl]-

Formula: C₁₃H₁₆FN

Purity: Min. 95%

Molecular weight: 205.27 g/mol

Ref: 3D-FF95966