60676-77-9 Usage
Description
N-(2-(1H-indole-3-yl) ethyl)-N-allylprop-2-en-1-aMine is a complex amine compound characterized by the presence of an indole ring and an allyl group. As an amine, it features a nitrogen atom bonded to alkyl or aryl groups, which contributes to its unique structure and properties. This chemical is a valuable building block for the synthesis of other molecules and holds potential therapeutic effects that are under investigation.
Uses
Used in Chemical Research:
N-(2-(1H-indole-3-yl) ethyl)-N-allylprop-2-en-1-aMine is used as a research chemical for its unique structure and properties, facilitating the development of new compounds and understanding of chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(2-(1H-indole-3-yl) ethyl)-N-allylprop-2-en-1-aMine is used as a precursor in the synthesis of pharmaceuticals, given its potential to contribute to the creation of novel therapeutic agents.
Used in Pharmacological Research:
N-(2-(1H-indole-3-yl) ethyl)-N-allylprop-2-en-1-aMine is utilized in pharmacological research to explore its potential therapeutic effects, which are currently under investigation, and to understand its interactions with biological systems.
Used in Drug Development:
N-(2-(1H-indole-3-yl) ethyl)-N-allylprop-2-en-1-aMine is used as a component in drug development, where its complex structure may offer new avenues for the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 60676-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,7 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60676-77:
(7*6)+(6*0)+(5*6)+(4*7)+(3*6)+(2*7)+(1*7)=139
139 % 10 = 9
So 60676-77-9 is a valid CAS Registry Number.
60676-77-9Relevant articles and documents
Design and synthesis of β-carboline and combretastatin derivatives as anti-neutrophilic inflammatory agents
Kumar, Sunil,Wang, Yi-Hsuan,Chen, Po-Jen,Chang, Yu-Chia,Kashyap, Hemant K.,Shen, Ya-Ching,Yu, Huang-Ping,Hwang, Tsong-Long
, (2021/04/09)
A series of β-carboline derivatives was synthesized by the Pictet-Spengler reaction with or without the combretastatin skeleton. The structures of these derivatives were elucidated by spectroscopic techniques. All synthesized compounds were evaluated for
Synthesis of tetrahydro-β-carbolines via isomerization of N-allyltryptamines: A metal-catalyzed variation on the Pictet-Spengler theme
Ascic, Erhad,Hansen, Casper L.,Le Quement, Sebastian T.,Nielsen, Thomas E.
supporting information; experimental part, p. 3345 - 3347 (2012/05/04)
An efficient and broadly applicable alternative to the classical Pictet-Spengler synthesis of tetrahydro-β-carbolines is presented. The method relies on metal-catalyzed isomerization of allylic amines to form reactive iminium intermediates which can be trapped by a tethered indole nucleophile. The Royal Society of Chemistry 2012.
