38843-82-2 Usage
Uses
Used in Research and Development:
1-(2,5-dimethoxyphenyl) pentan-1-one is used as a research chemical for studying the effects of psychoactive substances on the human brain and their potential applications in therapeutic settings. Its psychedelic properties make it a valuable tool for understanding the mechanisms of hallucinogenic drugs and their impact on mental health.
Used in Controlled Substances Regulation:
Due to its psychoactive properties, 1-(2,5-dimethoxyphenyl) pentan-1-one is considered a controlled substance in many countries. It is regulated under various drug laws to prevent misuse and ensure that its use is limited to research and medical purposes.
Used in Pharmaceutical Industry:
Although not directly used as a pharmaceutical product, 1-(2,5-dimethoxyphenyl) pentan-1-one may contribute to the development of new medications for the treatment of mental health disorders. Its study can provide insights into the effects of similar compounds and their potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 38843-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,4 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38843-82:
(7*3)+(6*8)+(5*8)+(4*4)+(3*3)+(2*8)+(1*2)=152
152 % 10 = 2
So 38843-82-2 is a valid CAS Registry Number.
38843-82-2Relevant academic research and scientific papers
P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis
Pandey, Ganesh,Tiwari, Sandip Kumar,Singh, Bhawana,Vanka, Kumar,Jain, Shailja
, p. 12337 - 12340 (2017/11/20)
p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.
Substituted 2-n-pentyl-1,4-naphthaquinones from 2-n-pentyl-1,4-benzoquinone and substituted 1,3-butadienes
Tandon, V. K.,Vaish, Meenu,Jain, P. K.
, p. 93 - 96 (2007/10/02)
Cycloaddition reaction of 2-n-pentyl-1,4-benzoquinone (6) with substituted 1,3-butadienes gives new 2-n-pentyl-1,4-dihydroxy-5,8-dihydronaphthalene derivatives (7).Oxidation of these cycloadducts gives the required 1,4-naphthaquinone derivatives (1).None
Psychotomimetic phenylisopropylamines. 5. 4 alkyl 2,5 dimethoxyphenylisopropylamines
Shulgin,Dyer
, p. 1201 - 1204 (2007/10/06)
A homologous series of 4 alkyl 2,5 dimethoxyphenylisopropylamines (alkyl = H through n C5H11 and t C4H9) was synthesized and compared with mescaline as serotonin agonists in a sheep umbilical preparation. The three carbon homolog 6d was found to be the most potent of the straight chain series in accordance with its observed psychotomimetic effectiveness in man.
