82830-44-2 Usage
Uses
Used in Scientific Research:
(+/-)-1-(2,5-DIMETHOXY-4-IODOPHENYL)-2-AMINOPROPANE HYDROCHLORIDE is used as a research chemical for studying the effects of psychedelic drugs on the brain and behavior. It aids in understanding the mechanisms of action and potential therapeutic applications of similar compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (+/-)-1-(2,5-DIMETHOXY-4-IODOPHENYL)-2-AMINOPROPANE HYDROCHLORIDE is used as a lead compound in the development of new medications targeting mental health conditions. Its study may contribute to the discovery of novel treatments for various psychiatric disorders.
Used in Therapeutic Exploration:
(+/-)-1-(2,5-DIMETHOXY-4-IODOPHENYL)-2-AMINOPROPANE HYDROCHLORIDE is used as a subject of investigation for its potential therapeutic effects on mental health conditions. Ongoing research aims to explore its efficacy and safety in treating specific disorders, potentially leading to new treatment options.
Check Digit Verification of cas no
The CAS Registry Mumber 82830-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,3 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82830-44:
(7*8)+(6*2)+(5*8)+(4*3)+(3*0)+(2*4)+(1*4)=132
132 % 10 = 2
So 82830-44-2 is a valid CAS Registry Number.
82830-44-2Relevant academic research and scientific papers
Behavioral and serotonin receptor properties of 4-substituted derivatives of the hallucinogen 1-(2,5-dimethoxyphenyl)-2-aminopropane
Glennon,Young,Benington,Morin
, p. 1163 - 1168 (2007/10/02)
The serotonin (5-HT) receptor affinities and behavioral (discriminative stimulus) properties of a series of 4-substituted derivatives of 1-(2,5-dimethoxyphenyl)-2-aminopropanes (2,5-DMA) were investigated. The substituents at the 4-position included H, OMe, OEt, Me, Et, F, Br, I, and NO2. Substituent lipophilicities (π values) of these functionalities appear to have a minimal effect on either 5-HT receptor affinity or behavioral activity. Those derivatives previously found to be most potent in human studies possess significant affinity for 5-HT receptors. Furthermore, when rats trained to discriminate (±)-1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) from saline were used, generalization was found to occur upon administration of the 4-substituted 2,5-DMA derivatives. Because a direct relationship exists between the ED50 values obtained from these discrimination studies and human hallucinogenic potencies, the discriminative stimulus paradigm, with DOM as a training drug, appears to be a useful tool for comparing the quantitative and qualitative (DOM-like) effects produced by certain hallucinogenic agents.
