33268-99-4 Usage
Uses
Used in Research Applications:
1-(1H-indol-3-yl)-N-methyl-1-phenylmethanamine is used as a research chemical for studying its psychoactive properties and potential effects on the central nervous system. 1-(1H-indol-3-yl)-N-methyl-1-phenylmethanamine's structure and interactions with biological systems provide valuable insights into the development of new therapeutic agents and understanding the mechanisms of psychoactive substances.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(1H-indol-3-yl)-N-methyl-1-phenylmethanamine may be used as a starting point for the development of new drugs targeting the central nervous system. Its structural features and psychoactive properties make it a candidate for further investigation and modification to create safer and more effective medications.
Check Digit Verification of cas no
The CAS Registry Mumber 33268-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,6 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33268-99:
(7*3)+(6*3)+(5*2)+(4*6)+(3*8)+(2*9)+(1*9)=124
124 % 10 = 4
So 33268-99-4 is a valid CAS Registry Number.
33268-99-4Relevant academic research and scientific papers
Diastereoselective synthesis of (2S*)-2-[(R*)-1H-indol-3-yl(phenyl)methyl]-2,3-dihydro-1H-inden-1-one
Semenov, Boris B.,Novikov, Kirill A.,Lysenko, Konstantin A.,Kachala, Vadim V.
, p. 3479 - 3483 (2007/10/03)
Double asymmetric induction in Michael reactions has been studied. Enantioselective alkylation of a cyclic ketone (1-indanone) with α-phenyl-nor-gramine was carried out. The relative configuration of (2S*)-2-[(R*)-1H-indol-3-yl(pheny
Diastereodirected alkylation of ketones and 1,3-diketones with N-[1H-Indol-3-yl(phenyl)methyl]-N-methylamine by the Michael reaction
Semenov,Smushkevich,Levina,Kurkovskaya,Lysenko,Kachala
, p. 730 - 738 (2007/10/03)
A method has been developed for introducing the 1H-indol-3-yl(phenyl)methyl residue into position 2 of ketones and 1,3-diketones. The principle of bringing in controlled diastereoselectivity based on the configuration of intermediates is demonstrated. 2005 Springer Science+Business Media, Inc.
