111963-87-2 Usage
Uses
Due to the limited information available on 5-METHOXY-3-(1-METHYL-4-PIPERIDINYL)INDOLE, it is difficult to provide a comprehensive list of its applications. However, based on the general properties of indole compounds, we can speculate on some potential uses in various industries:
Used in Pharmaceutical Industry:
5-METHOXY-3-(1-METHYL-4-PIPERIDINYL)INDOLE could be used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Indole-based compounds are often found in various drugs due to their diverse biological activities, such as their ability to interact with receptors, enzymes, or other biological targets.
Used in Chemical Research:
5-METHOXY-3-(1-METHYL-4-PIPERIDINYL)INDOLE may serve as a research compound for studying the structure-activity relationships of indole derivatives. Understanding how the presence of different functional groups affects the biological activity of indole compounds can help in the design of new drugs or other bioactive molecules.
Used in Material Science:
Indole compounds, including 5-METHOXY-3-(1-METHYL-4-PIPERIDINYL)INDOLE, could potentially be used in the development of new materials with unique properties. For example, they might be incorporated into polymers or other materials to impart specific characteristics, such as improved conductivity or enhanced stability.
Check Digit Verification of cas no
The CAS Registry Mumber 111963-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,6 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111963-87:
(8*1)+(7*1)+(6*1)+(5*9)+(4*6)+(3*3)+(2*8)+(1*7)=122
122 % 10 = 2
So 111963-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H20N2O/c1-17-7-5-11(6-8-17)14-10-16-15-4-3-12(18-2)9-13(14)15/h3-4,9-11,16H,5-8H2,1-2H3
111963-87-2Relevant academic research and scientific papers
Bonjoch, Josep,Boncompte, Fontsanta,Casamitjana, Nuria,Bosch, Joan
, p. 6693 - 6702 (1986)
The first synthesis of an indolomorphan system has been achieved through a route involving the acid-catalyzed cyclization of a 3-(tetrahydro-2-pyridyl)indoline.A procedure for the reduction of 3-(tetrahydropyridyl)indoles to the corresponding indolines, consisting in the formation of the tetrahydropyridine-borane complex followed by treatment with ethanolic hydrochloric acid, is established.
Synthesis of pharmacologically relevant indoles with amine side chains via tandem hydroformylation/fischer indole synthesis
Schmidt, Axel M.,Eilbracht, Peter
, p. 5528 - 5535 (2007/10/03)
The sequence of hydroformylation and Fischer indole synthesis starting from amino olefins and aryl hydrazines is described. In a convergent manner, the two units bearing pharmacologically relevant substituents are assembled in the final indolization step. This modular and diversity-oriented approach to tryptamines and homotryptamines can be conducted in water and allows synthesis of branched and nonbranched tryptamines as well as tryptamine-based pharmaceuticals such as the 5-HT1D agonist L 775 606.
5-HT1F agonists
-
, (2008/06/13)
The present invention relates to a compound of formula (I): or a pharmaceutical acid addition salt thereof; which is useful for activating 5-HT1freceptors and inhibiting protein extravasation in a mammal.
