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2(1H)-Quinolinone, 8-bromo-4-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54675-27-3

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54675-27-3 Usage

Chemical class

Quinolinone derivatives

Core structure

Quinoline core

Substituents

A hydroxy group and a bromo group attached to the core

Usage

Widely used in the chemical and pharmaceutical industries for the synthesis of various bioactive molecules, including potential drugs and agrochemicals

Biological activities

Exhibits antifungal and antibacterial properties

Additional potential effects

Has been studied for its potential antioxidant and anti-inflammatory effects, making it a promising candidate for the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 54675-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54675-27:
(7*5)+(6*4)+(5*6)+(4*7)+(3*5)+(2*2)+(1*7)=143
143 % 10 = 3
So 54675-27-3 is a valid CAS Registry Number.

54675-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-bromoquinoline-2,4-diol

1.2 Other means of identification

Product number -
Other names 8-Bromo-quinoline-2,4-diol

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:54675-27-3 SDS

54675-27-3Relevant academic research and scientific papers

ARYL / HETARYL SUBSTITUTED IMIDAZOQUINOLINES

-

Page 292, (2008/06/13)

Aryl substituted imidazoquinoline compounds, according to formula I, pharmaceutical compositions containing the compounds, intermediates, and methods of use of these compounds as immunomodulators, for inducing w or inhibiting cytokine biosynthesis in animals and in the treatment of diseases including viral., and neoplastic, are disclosed. formula (I): wherein: R is selected from the group consisting of alkyl, alkoxy, hydroxy, and trifluoromethyl;. N is 0 or 1; R3 is selected from the group consisting of: -Z-Ar,-Z-Ar’-Y-R4, -Z-Ar’-X-Y-R4, Z-Ar’-R5, and-Z-Ar'-X-R5; Ar is selected from the group consisting of aryl and heteroaryl both of which can be unsubstituted or can be substituted by one or more substituents independently selected from the group consisting of alkyl, alkenyl, alkoxy, methylenedioxy, haloalkyl, haloalkoxy, halogen, nitro, hydroxy, hydroxyalkyl, mercapto, cyano, carboxy, formyl, aryl, aryloxy, arylalkoxy, heteroaryl, heteroaryloxy, heteroarylalkoxy; heterocyctyl, heterocyclylalkyl, amino, alkylamino, and dialkylamino.

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