77092-19-4 Usage
Uses
Used in Research Applications:
4-MPD is utilized as a research chemical for the study of psychoactive substances and their effects on the central nervous system. It serves as a valuable tool in understanding the mechanisms of action of stimulant drugs and their potential for abuse.
Used in Forensic Analysis:
In forensic science, 4-MPD is identified and analyzed in cases involving drug abuse or illicit substance distribution. Its detection is crucial for law enforcement and regulatory agencies to enforce drug control policies and protect public health.
Used in Drug Policy and Regulation:
4-MPD is a key substance in the discourse on drug policy and regulation, as its classification as a controlled substance informs the legal framework surrounding the production, distribution, and consumption of psychoactive substances. This helps in the development of strategies to mitigate the risks associated with drug abuse and addiction.
Check Digit Verification of cas no
The CAS Registry Mumber 77092-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,9 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77092-19:
(7*7)+(6*7)+(5*0)+(4*9)+(3*2)+(2*1)+(1*9)=144
144 % 10 = 4
So 77092-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H18O5/c1-19(14-6-10-16(22-3)11-7-14)23-17(12-18(20)24-19)13-4-8-15(21-2)9-5-13/h4-12H,1-3H3
77092-19-4Relevant academic research and scientific papers
CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XXIII. REACTION OF 5-ARYL-2,3-DIHYDROFURAN-2,3-DIONES WITH ALDEHYDES AND KETONES
Andreichikov, Yu. S.,Gein, L. F.,Plakhina, G. D.
, p. 1995 - 1998 (2007/10/02)
5-Aryl-2,3-dihydrofuran-2,3-diones react with aldehydes, ketones, and α-ketoesters to form 2,2,5,6-tetrasubstituted 1,3-dioxen-4-ones.The reaction of 5-aryl-2,3-dihydrofuran-2,3-diones with α-diketones occurs either at one carbonyl group of the α-ketone to form 2,6-disubstituted 1,3-dioxen-4-ones or at both carbonyl groups to form 2,2',6,6'-tetrasubstituted 4,4'-dioxo-2,2'-bi(1,3-dioxenyls).