СоединенияОрганические соединения2-BROMO-1-PHENYL-PENTAN-1-ONE CAS 49851-31-2

What is 2 Bromo 1 phenyl pentan 1 one used for?

which can be used to prepare substituted imidazole derivatives with the following structure, which have high-efficiency KDM1A enzyme inhibitory activity and more than monoamine oxidase (MAO) selectivity, and can be used for histone demethylase activity Prevention or treatment of related diseases and disorders.

2-Bromo-1-phenylpentan-1-one is a chemical compound that is used in various applications. However, it is important to note that the compound you mentioned falls under the category of controlled substances in many jurisdictions due to its association with the production of illicit drugs, specifically substituted cathinones or “designer drugs.”

Substituted cathinones are a class of synthetic stimulant compounds that can have psychoactive effects when consumed. They are often sold under various street names and are known to have stimulant and hallucinogenic properties. However, the production, sale, possession, or distribution of substances like 2-bromo-1-phenylpentan-1-one for illicit purposes is illegal and subject to strict legal restrictions and regulations in most countries.

It is crucial to emphasize that the use of this compound or any related substances for illicit or illegal activities is strongly discouraged. This information is provided solely for educational purposes and to increase awareness about the compound. It is essential to comply with the laws and regulations of your country or region regarding controlled substances.

What is CAS number 49851 31 2?

The CAS number 49851-31-2 corresponds to a specific chemical compound known as N,N-Dimethyltryptamine-N-oxide. It is a derivative of N,N-Dimethyltryptamine (DMT), a naturally occurring hallucinogenic compound found in various plants and animals.

N,N-Dimethyltryptamine-N-oxide (CAS number 49851-31-2) is a less commonly studied compound compared to DMT itself. It is believed to be an oxidation product of DMT, resulting from the addition of an oxygen atom to the dimethyltryptamine molecule. However, its specific properties, effects, and applications are not extensively documented in the available scientific literature.