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3-bromo-2-(2-bromophenyl)quinolin-4(1H)-one is a complex organic compound with the molecular formula C15H8Br2NO. It is a derivative of quinolin-4(1H)-one, featuring a quinoline ring system with a 3-bromo substituent at the 3-position and a 2-bromophenyl group attached at the 2-position. 3-bromo-2-(2-bromophenyl)quinolin-4(1H)-one is characterized by its bromine atoms, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals and materials science. The presence of the bromine atoms also influences its physical properties, such as solubility and stability. The compound's structure and properties make it a subject of interest for researchers exploring the synthesis and applications of halogenated heterocyclic compounds.

5428-23-9

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5428-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5428-23-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5428-23:
(6*5)+(5*4)+(4*2)+(3*8)+(2*2)+(1*3)=89
89 % 10 = 9
So 5428-23-9 is a valid CAS Registry Number.

5428-23-9SDS

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 3-bromo-2-(2-bromophenyl)-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names 3-bromo-2-(2-bromophenyl)quinolin-4(1h)-one

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

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More Details:5428-23-9 SDS

5428-23-9Downstream Products

5428-23-9Relevant academic research and scientific papers

Heterocycle-heterocycle strategies: (2-nitrophenyl)isoxazole precursors to 4-aminoquinolines, 1 H-indoles, and quinolin-4(1 H)-ones

Coffman, Keith C.,Palazzo, Teresa A.,Hartley, Timothy P.,Fettinger, James C.,Tantillo, Dean J.,Kurth, Mark J.

supporting information, p. 2062 - 2065 (2013/06/05)

Reductive heterocycle-heterocycle (heterocycle → heterocycle; H-H) transformations that give 4-aminoquinolines, 3-acylindoles, and quinolin-4(1H)-ones from 2-nitrophenyl substituted isoxazoles are reported. When this methodology is applied to 3,5-, 4,5-,

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