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2,4-Dibromoquinoline-3-carboxaldehyde is a chemical compound with the molecular formula C11H6Br2NO. It is a derivative of quinoline, characterized by the presence of two bromine atoms and a carbaldehyde group. 2,4-Dibromoquinoline-3-carboxaldehyde is known for its strong fluorescence properties, which make it a valuable component in various applications.

532392-87-3

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532392-87-3 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dibromoquinoline-3-carboxaldehyde is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2,4-Dibromoquinoline-3-carboxaldehyde is used as a precursor in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Fluorescent Dyes:
2,4-Dibromoquinoline-3-carboxaldehyde is used as a component in the production of fluorescent dyes. Its strong fluorescence properties make it suitable for applications in research and diagnostics, where the detection and visualization of specific molecules or cells are required.
Used in Fluorescent Sensors and Probes:
2,4-Dibromoquinoline-3-carboxaldehyde is used as a key component in the development of fluorescent sensors and probes. These tools are essential for monitoring biological processes and environmental conditions, providing valuable insights into various scientific and medical fields.
Used in Cancer Research:
2,4-Dibromoquinoline-3-carboxaldehyde has been studied for its potential anti-cancer properties. It is used in research to explore its effects on cancer cells and to develop new therapeutic strategies for the treatment of various types of cancer.
Used in Anti-Inflammatory Research:
In addition to its potential anti-cancer properties, 2,4-Dibromoquinoline-3-carboxaldehyde is also being investigated for its anti-inflammatory effects. It is used in research to understand its role in modulating inflammation and to develop new treatments for inflammatory diseases.

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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