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Usage

Uses

Used in Recreational Purposes:
(5-chlorophenyl)isobutylamine is used as a recreational drug for its stimulant effects, which include increased alertness, energy, and euphoria. Its use is not approved for medical purposes and is subject to legal restrictions in some countries due to its potential for abuse and dependence.
Used in Research:
While not approved for medical use, (5-chlorophenyl)isobutylamine may be used in research settings to study the effects of psychoactive substances on the central nervous system. Its effects on the central nervous system are similar to those of amphetamines, which can include increased heart rate, elevated blood pressure, and improved focus and concentration.

Upstream product

• 121-73-3 3-Nitrochlorobenzene 
• 78-84-2 isobutyraldehyde 
• 108-42-9 3-chloro-aniline 

Downstream Products

• 139-24-2 (Z)-1,2-bis(3-chlorophenyl)diazene 1-oxide 

Relevant academic research and scientific papers

Catalytic Selective Oxidative Coupling of Secondary N-Alkylanilines: An Approach to Azoxyarene

Azoxyarenes are among important scaffolds in organic molecules. Direct oxidative coupling of primary anilines provides a concise fashion to construct them. However, whether these scaffolds can be prepared from secondary N-alkylanilines is not well explored. Here, we present a catalytic selective oxidative coupling of secondary N-alkylaniline to afford azoxyarene with tungsten catalyst under mild conditions. In addition, azoxy can be viewed as a bioisostere of alkene and amide. Several "azoxyarene analogues" of the corresponding bioactive alkenes and amides showed comparable promising anticancer activities.

EFFECT OF SUBSTITUENTS IN THE RING ON THE HYDROGENATION OF AROMATIC NITRO COMPOUNDS IN THE PRESENCE OF METAL COMPLEX CATALYSIS

In the presence of the complex of palladium with poly(4-vinylpyridine), grafted to the surface of polyethylene, the rates of hydrogenation of aromatic nitro compounds and of hydrogenation amination of 2-methylpropanal by aromatic nitro compounds depend on the nature of the substituent and decrease with increase in absolute value of the Hammett constant.