54752-30-6

Basic information

• Product Name: 1(2H)-Naphthalenone, 3,4-dihydro-2-[(4-methylphenyl)methylene]-
• CAS NO: 54752-30-6
• Molecular Formula: C18H16O
• Molecular Weight: 248.324
• Mol File: 54752-30-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1(2H)-Naphthalenone, 3,4-dihydro-2-[(4-methylphenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1(2H)-Naphthalenone, 3,4-dihydro-2-[(4-methylphenyl)methylene]-(54752-30-6)
• EPA Substance Registry System: 1(2H)-Naphthalenone, 3,4-dihydro-2-[(4-methylphenyl)methylene]-(54752-30-6)

Safety Data

• Hazardous Substances Data: 54752-30-6(Hazardous Substances Data)

Usage

General Description

1(2H)-Naphthalenone, 3,4-dihydro-2-[(4-methylphenyl)methylene]- is a chemical compound with the molecular formula C18H16O. It is a yellow crystalline solid that is commonly used in the production of pharmaceuticals, dyestuffs, and fragrance compounds. This chemical compound may also have potential applications in the field of organic synthesis and medicinal chemistry due to its unique structure and properties. Additionally, it is important to handle this compound with caution and follow proper safety protocols, as it may pose certain health risks if not handled properly.

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 

Downstream Products

• 78364-66-6 2-Bromo-2-(bromo-p-tolyl-methyl)-3,4-dihydro-2H-naphthalen-1-one 
• 1379762-78-3 (2R,3'S)-3'-(4-methphenyl)-3,4-dihydro-1H-spiro[naphthalene-2,2'-oxiran]-1-one 

Relevant articles and documents

Selectivity in the Aerobic Dearomatization of Phenols: Total Synthesis of Dehydronornuciferine by Chemo- and Regioselective Oxidation

We describe a selective aerobic oxidation of meta-biaryl phenols that enables rapid access to functionalized phenanthrenes. Aerobic oxidations attract interest due to their efficiency, but remain underutilized in complex molecule settings due to challenge

Antibacterial and antitubercular evaluation of dihydronaphthalenone-indole hybrid analogs

A new series of indole appended dihydronaphthalenone hybrid analogs (5a–t) have been synthesized through the Lewis acid catalyzed Michael addition of indoles to the arylidene/hetero arylidene ketones. All the synthesized derivatives are well characterized

UV-light induced domino type reactions: Synthesis and photophysical properties of unreported nitrogen ring junction quinazolines

An expedient method for the synthesis of 5,6-dihydrobenzo[h][1,2,4]triazolo[5,1-b]quinazolines by UV light has been developed. Our aim was to synthesize various α, β-unsaturated carbonyl compounds and to further react them with different amines in DMF, in