1213185-24-0 Usage
Description
(S)-2-methyl-1-(3,4,5-trimethoxyphenyl)propylamine is a chemical compound belonging to the class of propylamines. It is an enantiomer with a unique molecular structure, featuring a methyl group attached to the second carbon and a phenyl group with three methoxy substituents at the first carbon. (S)-2-methyl-1-(3,4,5-trimethoxyphenyl)propylamine has potential psychoactive properties and is being studied for its possible use in treating various diseases and conditions. Its potential applications in medicinal chemistry and drug development are of interest, but further research is required to fully comprehend its chemical properties and potential biological activities.
Uses
Used in Pharmaceutical Industry:
(S)-2-methyl-1-(3,4,5-trimethoxyphenyl)propylamine is used as a compound with potential psychoactive properties for the development of new medications targeting various diseases and conditions. Its unique molecular structure and potential effects on the central nervous system make it a promising candidate for further research and development in the pharmaceutical field.
Used in Medicinal Chemistry Research:
(S)-2-methyl-1-(3,4,5-trimethoxyphenyl)propylamine is used as a subject of study in medicinal chemistry to explore its chemical properties, potential biological activities, and possible applications in drug development. Understanding its interactions with biological systems and its effects on specific targets can lead to the creation of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1213185-24-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,1,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1213185-24:
(9*1)+(8*2)+(7*1)+(6*3)+(5*1)+(4*8)+(3*5)+(2*2)+(1*4)=110
110 % 10 = 0
So 1213185-24-0 is a valid CAS Registry Number.
1213185-24-0Relevant articles and documents
Alternative and complementary approaches to the asymmetric synthesis of C3 substituted NH free or N-substituted isoindolin-1-ones
Lamblin, Marc,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre
, p. 111 - 123 (2008/09/17)
Complementary synthetic approaches to enantiomerically pure C3 alkylated or arylated NH free or N-substituted isoindolinones have been developed. The key step is elaboration of diversely substituted 2-alkyl- and arylbenzylamines, which can be submitted to a bis-metallation process followed by interception with a carbonylating agent. They can be also converted into N-alkylbromobenzylcarbamates or into bromobenzyldicarbamates and the assembly of the titled compounds can be readily ensured by reliance upon the Parham cyclization process.
