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497084-46-5

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497084-46-5 Usage

General Description

3-Iodo-8-nitro-quinoline is a chemical compound with the molecular formula C9H5IN2O2. It is a yellow crystalline solid with a molecular weight of 302.05 g/mol. 3-Iodo-8-nitro-quinoline is often used in organic synthesis and medicinal chemistry as a starting material for the synthesis of various pharmaceuticals and agrochemicals. It has been reported to exhibit antibacterial and antifungal properties, making it a valuable compound for the development of new drugs. 3-Iodo-8-nitro-quinoline is also used as a reagent in chemical reactions such as the preparation of heterocyclic compounds and the modification of organic molecules. Its structure and properties make it a versatile and useful chemical in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 497084-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,0,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 497084-46:
(8*4)+(7*9)+(6*7)+(5*0)+(4*8)+(3*4)+(2*4)+(1*6)=195
195 % 10 = 5
So 497084-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H5IN2O2/c10-7-4-6-2-1-3-8(12(13)14)9(6)11-5-7/h1-5H

497084-46-5SDS

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 3-Iodo-8-nitroquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,3-iodo-8-nitro

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:497084-46-5 SDS

497084-46-5Relevant articles and documents

HETEROCYCLIC COMPOUND, APPLICATION THEREOF, AND COMPOSITION CONTAINING SAME

-

, (2022/03/07)

A heterocyclic compound represented by formula XI, a pharmaceutically acceptable salt, a solvate, or a solvate of a pharmaceutically acceptable salt thereof, use thereof, and a composition containing the same. The compound is novel in structure and has good STAT5 inhibitory activity.

Color-Tunable Light-up Bioorthogonal Probes for In Vivo Two-Photon Fluorescence Imaging

Dou, Yandong,Wang, Yajun,Duan, Yukun,Liu, Bin,Hu, Qinglian,Shen, Wei,Sun, Hongyan,Zhu, Qing

supporting information, p. 4576 - 4582 (2020/03/23)

Light-up bioorthogonal probes have attracted increasing attention recently due to their capability to directly image diverse biomolecules in living cells without washing steps. The development of bioorthogonal probes with excellent fluorescent properties

Halogen Bond-Assisted Electron-Catalyzed Atom Economic Iodination of Heteroarenes at Room Temperature

Kazi, Imran,Guha, Somraj,Sekar, Govindasamy

, p. 6642 - 6654 (2019/06/14)

A halogen bond-assisted electron-catalyzed iodination of heteroarenes has been developed for the first time under atom economic condition at room temperature. The iodination is successful with just 0.55 equiv of iodine and 0.50 equiv of peroxide. The kinetic study indicates that the reaction is elusive in the absence of a halogen bond between the substrate and iodine. The formation of a halogen bond, its importance in lowering the activation barrier for this reaction, the presence of radical intermediates in a reaction mixture, and the regioselectivity of the reaction have been demonstrated with several control experiments, spectroscopic analysis, and quantum chemical calculations. Allowing the formation of the halogen bond may offer a new strategy to generate the reactive radical intermediates and to enable the otherwise elusive electron-catalyzed reactions under mild reaction conditions.

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