90389-93-8

Usage

Uses

Used in Research and Development:
1-(3-iodophenyl)-N-methylmethanamine is used as a research chemical for the study of its psychoactive effects and potential interactions with the human brain's neurotransmitter systems. The application reason is to better understand the mechanisms of hallucinogenic substances and their impact on mental health, which could contribute to the development of new treatments for various psychiatric disorders.
Used in Forensic Analysis:
In the field of forensic science, 1-(3-iodophenyl)-N-methylmethanamine is used as a reference compound for the identification and analysis of designer drugs in criminal investigations. The application reason is to aid in the detection and prosecution of illegal drug manufacturing and distribution activities.
Used in Drug Policy and Regulation:
1-(3-iodophenyl)-N-methylmethanamine is also used in the development and enforcement of drug policy and regulation. The application reason is to establish legal frameworks and guidelines for the control and restriction of potentially harmful psychoactive substances, in order to protect public health and safety.

Upstream product

• 696-41-3 m-iodobenzaldehyde 
• 74-89-5 methylamine 
• 49617-83-6 m-Iodobenzyl bromide 

Downstream Products

• 954238-70-1 tert-butyl (3-iodobenzyl)(methyl)carbamate 
• 338998-85-9 C₁₆H₁₆INO 

Relevant academic research and scientific papers

Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors

Neuronal nitric oxide synthase (nNOS) inhibition is a promising strategy to treat neurodegenerative disorders, but the development of nNOS inhibitors is often hindered by poor pharmacokinetics. We previously developed a class of membrane-permeable 2-amino

Aryl-and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine and serotonin

The present invention relates to a method of treating disorders by administering to a patient in need of such treatment a therapeutically effective amount of a compound of formula (I): wherein R1-R8 are as described herein, R4 being aryl or heteroaryl.

Benzylamines: Synthesis and evaluation of antimycobacterial properties

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.