244615-50-7

Basic information

• Product Name: 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde
• Synonyms: 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde;4-(6-Hydroxynaphthalen-2-yl)benzaldehyde;6-(4-Formylphenyl)-2-naphthoic acid;4-(2-Naphthalenyl)-benzaldehyde
• CAS NO: 244615-50-7
• Molecular Formula: C19H14O3
• Molecular Weight: 232.28
• Mol File: 244615-50-7.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 409.9±24.0 °C(Predicted)
• Appearance: /
• Density: 1.158±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde(244615-50-7)
• EPA Substance Registry System: 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde(244615-50-7)

Safety Data

• Hazardous Substances Data: 244615-50-7(Hazardous Substances Data)

Usage

General Description

4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde is a chemical compound that belongs to the class of benzaldehyde derivatives. It is also known as 2-(4-carbomethoxy-6-formylnaphthalen-2-yl)benzaldehyde. 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde contains a benzene ring substituted with a naphthalene ring and an aldehyde group. It is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its chemical structure makes it an important intermediate in the production of complex organic molecules. Overall, 4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde plays a crucial role in the development of new chemical compounds with potential applications in various industries.

Upstream product

• 32316-92-0 naphthalene-2-boronic acid 
• 1122-91-4 4-bromo-benzaldehyde 
• 580-13-2 2-bromonaphthalene 
• 87199-17-5 4-formylphenylboronic acid, 
• 91-20-3 naphthalene 

Downstream Products

• 1580484-71-4 4-hydroxy-4-(4-(naphthalen-2-yl)phenyl)butan-2-one 

Relevant articles and documents

Nitrogen-containing compound, electronic component using same and electronic device

The invention belongs to the technical field of organic materials, and provides a nitrogen-containing compound, an electronic component using the same and an electronic device. The structure of the nitrogen-containing compound is shown as a formula I; in the formula I, Ar1 and Ar2 are independently selected from substituted or unsubstituted aryl with the carbon atom number of 6-25, L1 and L2 are independently selected from a single bond, substituted or unsubstituted arylene with the carbon atom number of 6-25 and the like; and the nitrogen-containing compound can effectively improve the performance of the electronic component.

Identification of C5-NH2 Modified Oseltamivir Derivatives as Novel Influenza Neuraminidase Inhibitors with Highly Improved Antiviral Activities and Favorable Druggability

Our previous efforts have proved that modifications targeting the 150-cavity of influenza neuraminidase can achieve more potent and more selective inhibitors. In this work, four subseries of C5-NH2 modified oseltamivir derivatives were designed

Novel π-conjugated molecules based on diimidazopyridine: Significantly improved the photophysical, thermal and electrochemical properties bearing different aryl substituents

A series of π-conjugated molecules based on diimidazolepyridine derivatives were designed, synthesized by Suzuki coupling reaction and cyclization reaction and characterized. Diimidazolepyridine motif as the main structure could improve the thermal stabil