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90679-35-9

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90679-35-9 Usage

General Description

5-Pyridin-4-yl-1H-indole is a chemical compound that has a pyridine ring attached to an indole group. It is commonly used as a building block in organic synthesis and pharmaceutical research. 5-PYRIDIN-4-YL-1H-INDOLE has been found to have potential therapeutic applications due to its ability to interact with biological systems. It is also known for its role as a ligand in coordination chemistry and its use in the development of new materials. Additionally, 5-Pyridin-4-yl-1H-indole has been studied for its potential use as a fluorescent probe for detecting various biomolecules and as a precursor for the synthesis of complex natural products.

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

90679-35-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-PYRIDIN-4-YL-1H-INDOLE

1.2 Other means of identification

Product number -
Other names 1H-INDOLE,5-(4-PYRIDINYL)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90679-35-9 SDS

90679-35-9Downstream Products

90679-35-9Relevant articles and documents

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 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.

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