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1,8-Naphthyridine-4-carbaldehyde is a heterocyclic aromatic aldehyde with the molecular formula C11H7NO. It features a naphthyridine ring system and a carbaldehyde functional group, making it a versatile chemical compound.

64379-46-0

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64379-46-0 Usage

Uses

Used in Pharmaceutical Industry:
1,8-Naphthyridine-4-carbaldehyde is used as a building block and intermediate in organic synthesis for the production of various pharmaceuticals. Its unique chemical properties allow for the creation of diverse drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1,8-naphthyridine-4-carbaldehyde serves as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Organic Material Synthesis:
1,8-Naphthyridine-4-carbaldehyde is utilized as a component in the synthesis of various organic materials, such as dyes, polymers, and other specialty chemicals, due to its reactive carbaldehyde group and aromatic nature.
Used as a Fluorescent Probe and Sensor:
Due to its unique chemical properties, 1,8-naphthyridine-4-carbaldehyde can be employed as a fluorescent probe and sensor for the detection of certain analytes. This application takes advantage of its ability to emit light upon interaction with specific substances, enabling sensitive and selective analytical techniques.
Used in the Development of Functional Materials:
1,8-Naphthyridine-4-carbaldehyde has potential applications in the development of functional materials, such as sensors, catalysts, and optoelectronic devices, owing to its versatile chemical structure and properties.
Used as a Research Tool in Chemical Biology:
As a research tool in chemical biology, 1,8-naphthyridine-4-carbaldehyde aids scientists in understanding biological processes and developing new therapeutic strategies by serving as a starting point for the synthesis of bioactive compounds and probes for biological studies.

Check Digit Verification of cas no

The CAS Registry Mumber 64379-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,7 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64379-46:
(7*6)+(6*4)+(5*3)+(4*7)+(3*9)+(2*4)+(1*6)=150
150 % 10 = 0
So 64379-46-0 is a valid CAS Registry Number.

64379-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-Naphthyridine-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1,8-naphthyridine-4-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:64379-46-0 SDS

64379-46-0Relevant academic research and scientific papers

Discovery of azetidinyl ketolides for the treatment of susceptible and multidrug resistant community-acquired respiratory tract infections

Magee, Thomas V.,Ripp, Sharon L.,Li, Bryan,Buzon, Richard A.,Chupak, Lou,Dougherty, Thomas J.,Finegan, Steven M.,Girard, Dennis,Hagen, Anne E.,Falcone, Michael J.,Farley, Kathleen A.,Granskog, Karl,Hardink, Joel R.,Huband, Michael D.,Kamicker, Barbara J.,Kaneko, Takushi,Knickerbocker, Michael J.,Liras, Jennifer L.,Marra, Andrea,Medina, Ivy,Nguyen, Thuy-Trinh,Noe, Mark C.,Obach, R. Scott,O'Donnell, John P.,Penzien, Joseph B.,Reilly, Usa Datta,Schafer, John R.,Shen, Yue,Stone, Gregory G.,Strelevitz, Timothy J.,Sun, Jianmin,Tait-Kamradt, Amelia,Vaz, Alfin D. N.,Whipple, David A.,Widlicka, Daniel W.,Wishka, Donn G.,Wolkowski, Joanna P.,Flanagan, Mark E.

experimental part, p. 7446 - 7457 (2010/06/13)

Respiratory tract bacterial strains are becoming increasingly resistant to currently marketed macrolide antibiotics. The current alternative telithromycin (1) from the newer ketolide class of macrolides addresses resistance but is hampered by serious safe

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