63720-48-9 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(3,5-dimethoxyphenyl)-2-phenylis utilized as a key intermediate in the synthesis of various pharmaceuticals and natural products. Its reactivity and structural features make it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Development:
Ethanone, 1-(3,5-dimethoxyphenyl)-2-phenylis employed as a building block in the development of new pharmaceuticals, particularly those targeting the central nervous system. Its psychoactive properties have been the subject of research, with the aim of understanding its potential therapeutic effects and applications in medicine.
Used in Research and Development:
Ethanone, 1-(3,5-dimethoxyphenyl)-2-phenylis used as a research compound in the study of its psychoactive properties and potential therapeutic effects. This helps in the exploration of new avenues for the treatment of various central nervous system disorders.
Used in Controlled Substances Regulation:
Due to its psychoactive properties and potential for abuse, Ethanone, 1-(3,5-dimethoxyphenyl)-2-phenylis subject to strict regulations in many countries. It is classified as a controlled substance, and its use is limited to specific applications under strict legal and regulatory frameworks.
Check Digit Verification of cas no
The CAS Registry Mumber 63720-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63720-48:
(7*6)+(6*3)+(5*7)+(4*2)+(3*0)+(2*4)+(1*8)=119
119 % 10 = 9
So 63720-48-9 is a valid CAS Registry Number.
63720-48-9Relevant academic research and scientific papers
Nazarov cyclization of divinyl and arylvinyl epoxides: Application in the synthesis of resveratrol-based natural products
Sudhakar, Gangarajula,Satish, Kovela
, p. 6475 - 6480 (2015/04/22)
New variation in the Nazarov cyclization has been developed by preparing divinyl and arylvinyl epoxides as pentadienyl cation precursors for the first time. Highly substituted cyclopentadienes, hydrindienes, and indenes were synthesized to demonstrate the compatibility of this reaction with substrates bearing a variety of substitutions and having different types of epoxides. Application of this method in the synthesis of resveratrol-based natural products was also demonstrated.
