1079-44-3 Usage
Description
2-(2,5-DIMETHYL-1H-INDOL-3-YL)-ETHYLAMINE is an organic compound with the chemical structure of an ethylamine derivative, featuring a 2,5-dimethyl-1H-indol-3-yl group attached to the nitrogen atom. 2-(2,5-DIMETHYL-1H-INDOL-3-YL)-ETHYLAMINE is known for its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
2-(2,5-DIMETHYL-1H-INDOL-3-YL)-ETHYLAMINE is used as a reactant in the total synthesis of (+)-minfiensine and related compounds via asymmetric cascade cyclization. This application is significant because (+)-minfiensine and its analogs have shown potential therapeutic effects in various medical conditions, making the synthesis of these compounds an important area of research.
In the context of the pharmaceutical industry, 2-(2,5-DIMETHYL-1H-INDOL-3-YL)-ETHYLAMINE serves as a key building block for the development of novel drugs with potential therapeutic benefits. Its role in the synthesis of (+)-minfiensine and related compounds highlights its importance in the discovery and creation of new pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1079-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1079-44:
(6*1)+(5*0)+(4*7)+(3*9)+(2*4)+(1*4)=73
73 % 10 = 3
So 1079-44-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2/c1-8-3-4-12-11(7-8)10(5-6-13)9(2)14-12/h3-4,7,14H,5-6,13H2,1-2H3
1079-44-3Relevant articles and documents
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Grandberg,Bobrova
, (1974)
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Asymmetric fluorinative dearomatization of tryptamine derivatives
Liang, Xiao-Wei,Liu, Chuan,Zhang, Wei,You, Shu-Li
supporting information, p. 5531 - 5534 (2017/07/07)
An asymmetric fluorinative dearomatization reaction of tryptamine derivatives was developed by using a chiral anion phase transfer catalyst (PTC) system, and the preliminary results of the reaction mechanistic study were achieved. This method is characterized by a simple operation, facile introduction of a fluorine atom in a highly enantioselective manner and construction of two contiguous quaternary stereogenic centers.