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532392-87-3

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532392-87-3 Usage

General Description

2,4-Dibromoquinoline-3-carboxaldehyde is a chemical compound with the molecular formula C11H6Br2NO. It is a derivative of quinoline and is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceuticals, agrochemicals, and fluorescent dyes. 2,4-Dibromoquinoline-3-carboxaldehyde is known for its strong fluorescence properties, making it useful in the development of fluorescent sensors and probes for biological and environmental applications. Additionally, 2,4-Dibromoquinoline-3-carboxaldehyde has been studied for its potential anti-cancer and anti-inflammatory properties, further highlighting its importance in medicinal and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 532392-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,3,9 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 532392-87:
(8*5)+(7*3)+(6*2)+(5*3)+(4*9)+(3*2)+(2*8)+(1*7)=153
153 % 10 = 3
So 532392-87-3 is a valid CAS Registry Number.

532392-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibromoquinoline-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,4-Dibromoquinoline-3-carboxaldehyde

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:532392-87-3 SDS

532392-87-3Relevant articles and documents

Regioselective Sonogashira couplings of 2,4-dibromoquinolines. A correction

Nolan, Jason M.,Comins, Daniel L.

, p. 3736 - 3738 (2007/10/03)

Heteronuclear multiple bond correlation (HMBC) was used to determine the regiochemical outcome of palladium-catalyzed carbon-carbon bond formation between 2,4-dibromoquinolines and terminal acetylenes. The observed regioselectivity of these coupling react

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