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 
• 91-20-3 naphthalene 
• 580-13-2 2-bromonaphthalene 
• 87199-17-5 4-formylphenylboronic acid, 

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.

Ceramic boron carbonitrides for unlocking organic halides with visible light

Photochemistry provides a sustainable pathway for organic transformations by inducing radical intermediates from substrates through electron transfer process. However, progress is limited by heterogeneous photocatalysts that are required to be efficient, stable, and inexpensive for long-term operation with easy recyclability and product separation. Here, we report that boron carbonitride (BCN) ceramics are such a system and can reduce organic halides, including (het)aryl and alkyl halides, with visible light irradiation. Cross-coupling of halides to afford new C-H, C-C, and C-S bonds can proceed at ambient reaction conditions. Hydrogen, (het)aryl, and sulfonyl groups were introduced into the arenes and heteroarenes at the designed positions by means of mesolytic C-X (carbon-halogen) bond cleavage in the absence of any metal-based catalysts or ligands. BCN can be used not only for half reactions, like reduction reactions with a sacrificial agent, but also redox reactions through oxidative and reductive interfacial electron transfer. The BCN photocatalyst shows tolerance to different substituents and conserved activity after five recycles. The apparent metal-free system opens new opportunities for a wide range of organic catalysts using light energy and sustainable materials, which are metal-free, inexpensive and stable. This journal is

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