90679-35-9 Usage
Uses
Used in Pharmaceutical Research:
5-Pyridin-4-yl-1H-indole is used as a building block in the development of new pharmaceutical compounds, leveraging its chemical properties to create novel therapeutic agents.
Used in Organic Synthesis:
As a key intermediate, 5-Pyridin-4-yl-1H-indole is utilized in organic synthesis for the creation of a variety of chemical products, taking advantage of its reactive sites for further functionalization.
Used in Coordination Chemistry:
5-Pyridin-4-yl-1H-indole serves as a ligand in coordination chemistry, forming complexes with metal ions that can have applications in catalysis, sensing, and material science.
Used in Material Development:
5-PYRIDIN-4-YL-1H-INDOLE is employed in the development of new materials, potentially contributing to advances in areas such as electronics, optoelectronics, and nanotechnology due to its electronic and structural properties.
Used in Fluorescent Probe Development:
5-Pyridin-4-yl-1H-indole is used as a fluorescent probe for detecting various biomolecules, capitalizing on its fluorescent properties to visualize and study biological processes at the molecular level.
Used in Natural Product Synthesis:
As a precursor, 5-Pyridin-4-yl-1H-indole aids in the synthesis of complex natural products, facilitating the production of bioactive compounds with potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 90679-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,7 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90679-35:
(7*9)+(6*0)+(5*6)+(4*7)+(3*9)+(2*3)+(1*5)=159
159 % 10 = 9
So 90679-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2/c1-2-13-12(5-8-15-13)9-11(1)10-3-6-14-7-4-10/h1-9,15H
90679-35-9Relevant academic research and scientific papers
Rapid Syntheses of Heteroaryl-Substituted Imidazo[1,5-a]indole and Pyrrolo[1,2-c]imidazole via Aerobic C2-H Functionalizations
Kong, Wei-Jun,Chen, Xingrong,Wang, Mingming,Dai, Hui-Xiong,Yu, Jin-Quan
supporting information, p. 284 - 287 (2018/01/17)
Here we report an aerobic Pd(0) catalyzed C2-H functionalization of indoles and pyrroles with tethered N-methoxylamide as the directing group. A Pd(0)-initiated mechanism overcomes the directing or poisoning effect from a wide range of heterocycles including pyridine, pyrimidine, and thiazole. The imidazo[1,5-a]indole products are transformed to bioactive analogs after one-step manipulations, demonstrating the potential utility of this reaction in drug discovery.
NOVEL 2,3-DIHYDROINDOLE COMPOUNDS
-
Page/Page column 8, (2008/06/13)
The invention relates to compounds of the formula I wherein the variables are as defined in the claims. The compounds are useful in the treatment of a disease where a D4 receptor and/or a 5-HT 2A receptor is implicated.
NOVEL 2,3-DIHYDROINDOLE COMPOUNDS
-
Page/Page column 21-22, (2010/11/26)
The invention relates to compounds of the formula I, wherein the variables are as defined in the claims. The compounds are useful in the treatment of a disease where a D4 receptor and/or a 5-HT2A receptor is implicated.
SYNTHESIS OF 5-ARYLATED INDOLES VIA PALLADIUM-CATALYZED CROSS-COUPLING REACTION OF 5-INDOLYLBORONIC ACID WITH ARYL AND HETEROARYL HALIDES
Yang, Youhua,Martin, Arnold R.
, p. 1395 - 1398 (2007/10/02)
Palladium(0)-catalyzed cross-coupling reaction of 5-indolylboronic acid with various aryl and heteroaryl halides results in regioselective formation of 5-arylated indoles in good yields.
