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4-Chloroquinoline-6-carbaldehyde is a chemical compound characterized by the molecular formula C10H6ClNO. It is a derivative of quinoline, featuring a chlorine atom and an aldehyde group. 4-Chloroquinoline-6-carbaldehyde is recognized for its versatility as a building block in the synthesis of various products, including pharmaceuticals, agrochemicals, and dyes. Its potential biological activities, such as antifungal and antibacterial properties, have also been a subject of study. Furthermore, 4-Chloroquinoline-6-carbaldehyde has been explored for its role in the development of fluorescent dyes and materials for organic electronics, highlighting its broad applications in chemistry and material science.

676256-25-0

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676256-25-0 Usage

Uses

Used in Pharmaceutical Synthesis:
4-Chloroquinoline-6-carbaldehyde is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and reactivity.
Used in Agrochemical Production:
In the agrochemical industry, 4-Chloroquinoline-6-carbaldehyde serves as a building block for the creation of various agrochemicals, potentially enhancing crop protection and yield.
Used in Dye Manufacturing:
4-Chloroquinoline-6-carbaldehyde is employed as a precursor in the manufacturing of dyes, where its chemical properties allow for the production of a range of colorants used in different industries.
Used in Research for Biological Activities:
4-Chloroquinoline-6-carbaldehyde is used as a subject of research for its potential antifungal and antibacterial properties, indicating its possible use in antimicrobial applications.
Used in the Development of Fluorescent Dyes:
4-Chloroquinoline-6-carbaldehyde is applied in the research and development of fluorescent dyes, which have uses in various fields such as bioimaging and diagnostics.
Used in Organic Electronics:
4-Chloroquinoline-6-carbaldehyde is utilized in the development of materials for organic electronics, potentially contributing to advancements in flexible electronics and other related technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 676256-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,2,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 676256-25:
(8*6)+(7*7)+(6*6)+(5*2)+(4*5)+(3*6)+(2*2)+(1*5)=190
190 % 10 = 0
So 676256-25-0 is a valid CAS Registry Number.

676256-25-0SDS

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 4-chloroquinoline-6-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Chloro-quinoline-6-carbaldehyde

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:676256-25-0 SDS

676256-25-0Relevant academic research and scientific papers

NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING

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Paragraph 00563, (2018/11/22)

The present invention provides small-molecule inhibitors of BMP signaling and compositions and methods for inhibiting BMP signaling. These compounds and compositions may be used to modulate cell growth, differentiation, proliferation, and apoptosis, and thus may be useful for treating diseases or conditions associated with BMP signaling, including inflammation, cardiovascular disease, hematological disease, cancer, and bone disorders, as well as for modulating cellular differentiation and/or proliferation. These compounds and compositions may also be used to treat subjects with Sjogren's syndrome, or diffuse intrinsic pontine glioma (DIPG).

THIAZOLIDINONE COMPOUNDS, AND METHODS OF MAKING AND USING SAME

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Page/Page column 25, (2009/04/25)

Provided herein are thiazolidinone compounds, and methods of making and using the same. Such compounds may be used in inflammatory or immune-mediated disorders. The disclosure provides for treating respiratory or ocular disorders, treating arthritis, or may be used to treat cancer, such as prostate or breast cancer, or multiple myeloma.

THIAZOLONES FOR USE AS PI3 KINASE INHIBITORS

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, (2008/06/13)

Invented is a method of inhibiting the activity/function of PI3 kinases using substituted thiazolones. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, ne

THIAZOLIDINEDIONE DERIVATIVES AS PI3 KINASE INHIBITORS

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, (2008/06/13)

Invented is a method of inhibiting the activity/function of PI3 kinases using thiazolidinedione derivatives. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, allergy, asthma, pancreatitis, multiorgan failure, kidney diseases, platelet aggregation, cancer, sperm motility, transplantation rejection, graft rejection and lung injuries by the administration of thiazolidinedione derivatives.

Thiazolinone 4-monosubstituted quinolines

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Page/Page column 14; 31, (2010/10/20)

Thiazolinone monosubstituted quinoline derivatives where the quinoline ring is mono-substituted at the 4 positions which derivatives demonstrates CDK1 antiproliferative activity and are useful as anti-cancer agents.

NOVEL CHEMICAL COMPOUNDS

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, (2010/11/25)

This invention relates to newly identified compounds for inhibiting hYAK3 proteins and methods for treating diseases associated with hYAK3 activity.

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