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2-Bromoquinoline-4-carboxaldehyde is a chemical compound characterized by its molecular formula C10H6BrNO. It is a yellow to orange solid with a molecular weight of 237.07 g/mol. 2-BROMOQUINOLINE-4-CARBOXALDEHYDE is recognized for its role as a building block in the synthesis of various products, including pharmaceuticals, agrochemicals, and dyes. Additionally, it serves as a reagent in organic synthesis and as a fluorescent labeling reagent for the detection of biological molecules. Due to its hazardous nature, it is essential to handle 2-Bromoquinoline-4-carboxaldehyde with care to avoid skin and eye irritation.

866831-75-6

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866831-75-6 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromoquinoline-4-carboxaldehyde is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of a wide range of medicinal compounds with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromoquinoline-4-carboxaldehyde is utilized as a component in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products helps enhance their effectiveness in protecting crops and controlling pests, thereby contributing to increased agricultural productivity.
Used in Dye Industry:
2-Bromoquinoline-4-carboxaldehyde is employed as a building block in the production of dyes, which are used in various applications, including textiles, plastics, and printing inks. Its distinctive color properties enable the creation of a diverse array of dyes with specific characteristics, catering to the needs of different industries.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2-Bromoquinoline-4-carboxaldehyde plays a crucial role in facilitating various chemical reactions. Its presence can help drive the synthesis of complex organic molecules, which can be further utilized in the development of new compounds and materials.
Used in Biological Research:
2-Bromoquinoline-4-carboxaldehyde is used as a fluorescent labeling reagent for the detection and analysis of biological molecules. Its fluorescent properties allow researchers to track and visualize specific biomolecules within biological systems, aiding in the study of their functions and interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 866831-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,8,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 866831-75:
(8*8)+(7*6)+(6*6)+(5*8)+(4*3)+(3*1)+(2*7)+(1*5)=216
216 % 10 = 6
So 866831-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H6BrNO/c11-10-5-7(6-13)8-3-1-2-4-9(8)12-10/h1-6H

866831-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoquinoline-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Quinolinecarboxaldehyde,2-bromo

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:866831-75-6 SDS

866831-75-6Downstream Products

866831-75-6Relevant academic research and scientific papers

Regioselective lithium-halogen exchange and palladium-catalyzed cross-coupling reactions of 2,4-dihaloquinolines

Comins, Daniel L.,Nolan, Jason M.,Bori, Ibrahim D.

, p. 6697 - 6699 (2005)

Lithium-halogen exchange of 2,4-dibromoquinolines proceeds regioselectively at C-4 and affords 4-substituted quinolines on quenching with electrophiles. Palladium-catalyzed cross-coupling reactions of 2-bromo-4-iodoquinoline provide 4-substituted 2-bromoq

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