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1H-Imidazo[4,5-g]quinoline, also known as 1H-imidazo[4,5-g]quinoline(8CI,9CI), is a heterocyclic organic compound with the molecular formula C13H9N. It is a member of the imidazoquinoline family, which are fused-ring systems consisting of an imidazole and a quinoline. 1H-Imidazo[4,5-g]quinoline(8CI,9CI) is of interest in medicinal chemistry due to its potential biological activities, such as antiviral and anticancer properties. It has been studied for its ability to inhibit certain enzymes and receptors, which could make it a candidate for drug development. The compound is also known for its fluorescent properties, which can be useful in various analytical techniques. Despite its potential applications, it is important to note that the safety and efficacy of 1H-imidazo[4,5-g]quinoline in humans have not been fully established, and further research is needed to explore its therapeutic potential.

269-08-9

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269-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 269-08-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 269-08:
(5*2)+(4*6)+(3*9)+(2*0)+(1*8)=69
69 % 10 = 9
So 269-08-9 is a valid CAS Registry Number.

269-08-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-imidazo[4,5-g]quinoline

1.2 Other means of identification

Product number -
Other names Imidazo<4,5-g>chinolin

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:269-08-9 SDS

269-08-9Downstream Products

269-08-9Relevant academic research and scientific papers

Diversified facile synthesis of benzimidazoles, quinazolin-4(3H)-ones and 1,4-benzodiazepine-2,5-diones via palladium-catalyzed transfer hydrogenation/condensation cascade of nitro arenes under microwave irradiation

Zhu, Kaicheng,Hao, Jian-Hong,Zhang, Cheng-Pan,Zhang, Jiajun,Feng, Yiqing,Qin, Hua-Li

, p. 11132 - 11135 (2015/03/05)

A highly efficient diversified methodology for preparation of benzimidazole, quinazolin-4(3H)-ones and 1,4-benzodiazepine-2,5-diones is established using a palladium-catalyzed transfer hydrogenation (CTH)/condensation cascade of o-nitroaniline and o-nitrobenzamides in a triethylamine-formic acid azeotropic mixture (2:5) under microwave irradiation.

Quinoline tricyclic derivatives. Design, synthesis and evaluation of the antiviral activity of three new classes of RNA-dependent RNA polymerase inhibitors

Carta, Antonio,Briguglio, Irene,Piras, Sandra,Corona, Paola,Boatto, Giampiero,Nieddu, Maria,Giunchedi, Paolo,Marongiu, Maria Elena,Giliberti, Gabriele,Iuliano, Filippo,Blois, Sylvain,Ibba, Cristina,Busonera, Bernardetta,La Colla, Paolo

, p. 7070 - 7084 (2012/01/03)

In this study three new classes of linear N-tricyclic compounds, derived by condensation of the quinoline nucleus with 1,2,3-triazole, imidazole or pyrazine, were synthesized, obtaining triazolo[4,5-g]quinolines, imidazo[4,5-g]quinolines and pyrido[2,3-g]

Synthesis of two novel tricyclic rings: Triazolo[4,5-g]- quinolines and pyrido[2,3-g]quinoxalines derived from 6,7-diaminoquinolines

Sanna, Paolo,Carta, Antonio,Paglietti, Giuseppe

, p. 423 - 432 (2007/10/03)

A general simple route for the synthesis of triazolo[4,5-g]quinolines and pyrido[2,3-g]quinoxalines is described. The heterocycles obtained were fully characterised by their spectroscopical properties. A revision of the nitration of the 2,3-dichloroacetanilide is also discussed, since it afforded the request nitro derivative to build up the key intermediate 6,7- diaminoquinolines.

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