91295-74-8 Usage
Description
ATM4 4-Acetoxy Analog is an acetylated product derived from thebaine, an endogenous alkaloid found in opium. It is an analytical reference standard and a potential impurity in the synthesis of heroin. ATM4 4-Acetoxy Analog has been identified in seized heroin samples and is intended for research and forensic applications.
Uses
Used in Illicit Drug Synthesis:
ATM4 4-Acetoxy Analog is used as an impurity in the synthesis of illicit heroin. It is a byproduct of the acetylation process that converts morphine to heroin, and its presence in heroin samples can be analyzed for forensic purposes.
Used in Research and Forensic Applications:
ATM4 4-Acetoxy Analog is utilized as an analytical reference standard in research and forensic investigations. Its identification in heroin samples can provide valuable information on the synthesis process and the presence of other impurities, aiding in the understanding of drug trafficking and substance abuse issues.
Check Digit Verification of cas no
The CAS Registry Mumber 91295-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,9 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91295-74:
(7*9)+(6*1)+(5*2)+(4*9)+(3*5)+(2*7)+(1*4)=148
148 % 10 = 8
So 91295-74-8 is a valid CAS Registry Number.
91295-74-8Relevant articles and documents
Thebaine Rearrangements: Nonclassical D Ring Migrations
Allen, Andrew C.,Cooper, Donald A.,Moore, James M.,Teer, Charles B.
, p. 3462 - 3465 (2007/10/02)
3,6-Dimethoxy-4-acetoxy-5-phenanthrene (3) and its isomer 3,6-dimethoxy-4-acetoxy-8-phenanthrene (4) have been detected as manufacturing byproducts at trace levels in illicit heroin.These compounds are novel rearrangement products obtained by the action of acetic anhydride (Ac2O) on thebaine (1).The syntheses of 3 and 4 from 1 proceed via the intermediate Δ5,7,9(14)-N-acetyldesthebaine (2).Structural characterization and optimization of synthetic conditions for 3 and 4 are described.A brief discussion is also giving concerning other neutral products of 1 obtained under Ac2O conditions.
