4083-58-3

Basic information

• Product Name: 2,4-Dimethylpentan-3-amine hydrochloride
• Synonyms: 2,4-Dimethylpentan-3-amine hydrochloride
• CAS NO: 4083-58-3
• Molecular Formula: C7H18ClN
• Molecular Weight: 151.67752
• Mol File: 4083-58-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2,4-Dimethylpentan-3-amine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Dimethylpentan-3-amine hydrochloride(4083-58-3)
• EPA Substance Registry System: 2,4-Dimethylpentan-3-amine hydrochloride(4083-58-3)

Safety Data

• Hazardous Substances Data: 4083-58-3(Hazardous Substances Data)

Usage

General Description

2,4-Dimethylpentan-3-amine hydrochloride is a chemical compound with the molecular formula C7H17ClN. It is also known as 2,4-Dimethyl-3-pentanamine hydrochloride and is a derivative of amphetamine. 2,4-Dimethylpentan-3-amine hydrochloride is a psychoactive drug with stimulant effects and is used for its central nervous system stimulant properties. It acts as a norepinephrine-dopamine releasing agent, increasing the levels of these neurotransmitters in the brain. It is often used as a recreational drug and has a potential for abuse and addiction. 2,4-Dimethylpentan-3-amine hydrochloride is typically found in the form of a white crystalline powder and is commonly consumed orally, intranasally, or by injection.

Upstream product

• 108-08-7 2,4-dimethylpentane 

Relevant articles and documents

Cerium-Catalyzed C-H Functionalizations of Alkanes Utilizing Alcohols as Hydrogen Atom Transfer Agents

Modern photoredox catalysis has traditionally relied upon metal-to-ligand charge-transfer (MLCT) excitation of metal polypyridyl complexes for the utilization of light energy for the activation of organic substrates. Here, we demonstrate the catalytic application of ligand-to-metal charge-transfer (LMCT) excitation of cerium alkoxide complexes for the facile activation of alkanes utilizing abundant and inexpensive cerium trichloride as the catalyst. As demonstrated by cerium-catalyzed C-H amination and the alkylation of hydrocarbons, this reaction manifold has enabled the facile use of abundant alcohols as practical and selective hydrogen atom transfer (HAT) agents via the direct access of energetically challenging alkoxy radicals. Furthermore, the LMCT excitation event has been investigated through a series of spectroscopic experiments, revealing a rapid bond homolysis process and an effective production of alkoxy radicals, collectively ruling out the LMCT/homolysis event as the rate-determining step of this C-H functionalization.