38847-94-8 Usage
Uses
Used in Research and Development:
[1-(1,3-Benzodioxol-5-ylacetyl)-2-pyrrolidinyl]methanol is used as a research chemical for the study of its psychoactive effects and potential applications in the field of neuroscience. [1-(1,3-Benzodioxol-5-ylacetyl)-2-pyrrolidinyl]methanol serves as a valuable tool for researchers to understand the interactions and mechanisms related to its psychoactive properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [1-(1,3-Benzodioxol-5-ylacetyl)-2-pyrrolidinyl]methanol may be used as a starting material or intermediate in the synthesis of other compounds with potential therapeutic applications. Its unique chemical structure could be exploited to develop new drugs targeting specific receptors or pathways in the body.
Used in Forensic Science:
[1-(1,3-Benzodioxol-5-ylacetyl)-2-pyrrolidinyl]methanol, being a designer drug, may be encountered in forensic science for the analysis and identification of substances related to drug abuse or criminal investigations. Its detection and analysis can help in understanding the prevalence and distribution of designer drugs in society.
Check Digit Verification of cas no
The CAS Registry Mumber 38847-94-8 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 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38847-94:
(7*3)+(6*8)+(5*8)+(4*4)+(3*7)+(2*9)+(1*4)=168
168 % 10 = 8
So 38847-94-8 is a valid CAS Registry Number.
38847-94-8Relevant academic research and scientific papers
Stereoselective Gold(I)-Catalyzed Vinylcyclopropanation via Generation of a Sulfur-Substituted Vinyl Carbene Equivalent
Yuan, Tengrui,Ryckaert, Bram,Van Hecke, Kristof,Hullaert, Jan,Winne, Johan M.
supporting information, p. 4070 - 4074 (2020/12/22)
A stereoselective gold(I)-catalyzed vinylcyclopropanation of alkenes has been developed. A gold-coordinated cationic vinyl carbene species, readily generated via a rearrangement of the ethylenedithioacetal of propargyl aldehyde, reacts with a wide range of alkenes to afford thio-substituted vinylcyclopropanes. The gold-catalyzed vinyl cyclopropanation proceeds under mild conditions at room temperature and is generally selective for the formation of cis-substituted cyclopropanes. The reaction allows the formal introduction of a “naked” vinyl carbene, by subsequent chemoselective hydrodesulfurisation of the ethylenedithio-bridge. The synthetic utility of the new method is demonstrated by a short, racemic formal synthesis of the alkaloid cephalotaxin, hinging on a key vinyl cyclopropane-cyclopentene rearrangement.
