1206614-03-0 Usage
Description
2-[4-Methoxy-3-(phenylMethoxy)phenyl]-1-(1-pyrrolidinyl)ethanone is a complex organic compound characterized by its unique molecular structure and brown oil appearance. It is a derivative of ethanone with a pyrrolidinyl group and a substituted phenyl ring, which contributes to its distinct chemical properties.
Uses
Used in Pharmaceutical Industry:
2-[4-Methoxy-3-(phenylMethoxy)phenyl]-1-(1-pyrrolidinyl)ethanone is used as an intermediate in the synthesis of (S)-Reticuline, a key compound in the production of various alkaloids and pharmaceuticals. Its role in the preparation of (S)-Reticuline is crucial for the development of medications with potential therapeutic applications.
Used in Chemical Research:
As a brown oil, 2-[4-Methoxy-3-(phenylMethoxy)phenyl]-1-(1-pyrrolidinyl)ethanone serves as a valuable subject for chemical research, particularly in the study of organic synthesis, reaction mechanisms, and the development of novel chemical processes. Its unique structure and properties make it an interesting candidate for further exploration and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1206614-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,6,1 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1206614-03:
(9*1)+(8*2)+(7*0)+(6*6)+(5*6)+(4*1)+(3*4)+(2*0)+(1*3)=110
110 % 10 = 0
So 1206614-03-0 is a valid CAS Registry Number.
1206614-03-0Relevant articles and documents
Enantioselective syntheses and X-ray structures of (S)- and (R)-N-norlaudanidine: trace opium constituents
Zein, Ahmed L.,Dakhil, Otman O.,Dawe, Louise N.,Georghiou, Paris E.
scheme or table, p. 177 - 180 (2010/03/04)
The enantioselective synthesis of each of the enantiomers of N-norlaudanidine, a minor Papaver somniferum opium benzyltetrahydoisoquinoline alkaloid is described. This was achieved using a chiral auxiliary-mediated Bischler-Napieralski cyclization-sodium borohydride reduction strategy. The X-ray crystal structures of each of these secondary amines are reported.
